NZ791336A - 7-substituted sulfonimidoylpurinone compounds for the treatment and prophylaxis of virus infection - Google Patents

Abstract

The present invention relates to compounds of formula (I), wherein R1, R2 and R3 are as described herein, and their prodrugs or pharmaceutically acceptable salt, enantiomer or diastereomer thereof, and compositions including the compounds and methods of using the compounds as TLR7 agonists for the treatment of viral infections. reatment of viral infections.

Description

tituted sulfonimidoylpurinone compounds for the treatment and prophylaxis of virus infection This application is a divisional of New Zealand patent application 750604, which is the national phase entry in New Zealand of PCT international application (published as The present invention relates to novel sulfonimidoylpurinones derivatives that have in vivo Toll-like receptor m activity, as well as their manufacture, ceutical compositions containing them and their potential use as medicaments.

FIELD OF THE INVENTION The present invention relates to compounds of a (I), (I), n R1 to R3 are described below, or pharmaceutically acceptable salt, enantiomer or diastereomer thereof.

Toll-like receptors (TLRs) detect a wide range of ved pathogen-associated molecular patterns (PAMPs). They play an important role of sensing invading pathogens and subsequent initiation of innate immune responses. There are 10 known members of the TLR family in human, which are type I transmembrane proteins featuring an extracellular e-rich domain and a cytoplasmic tail that contains a conserved Toll/ interleukin (IL)-1 receptor (TIR) domain.

Within this family, TLR3, TLR7, TLR8 and TLR9 are located within endosomes. TLR7 can be ted by binding to a specific small molecule ligand (i.e., TLR7 agonist) or its native ligand (i.e., single-stranded RNA, ssRNA). ing binding of ssRNA to TLR7, the receptor in its dimerized form is believed to undergo a structural change leading to the subsequent recruitment of adapter proteins at its cytoplasmic domain, including the myeloid differentiation primary response gene 88 (MyD88). Following the initiation of the receptor signalling cascade via the MyD88 pathway, cytoplasmic transcription factors such as interferon regulatory factor 7 (IRF-7) and nuclear factor kappa B (NF-κB) are activated. These transcription factors then translocate to the nucleus and initiate the transcription of various genes, e.g., IFN-α and other antiviral ne genes. TLR7 is predominately expressed on plasmacytoid cells, and also on B-cells.

Altered responsiveness of immune cells might contribute to the reduced innate immune responses during chronic viral infections. Agonist-induced activation of TLR7 might therefore represent a novel approach for the treatment of chronic viral infections. (D. J Connolly and L. AJ O’Neill, Current Opinion in Pharmacology 2012, -518, P. A. Roethle et al, J. Med. Chem. 2013, 56, 7324-7333).

The current therapy of chronic HBV infection is based on two different types of drugs: the traditional ral nucleos(t)ide analogues and the more recent ted IFN-α (PEG-IFN-α).

The oral s(t)ide analogues act by suppressing the HBV replication. This is a life-long course of treatment during which drug resistance often occurs. As an alternative option, Pegylated IFN-α (PEG-IFN-α) has been used to treat some chronic ed HBV patients within finite therapy duration. Although it has achieved seroconversion in HBeAg at least in a small percentage of HBV patients, the e effect makes it poorly tolerable. Notably, functional cure defined as HBsAg seroconversion is very rare with both current therapies. A new generation therapeutic option to treat HBV patients for a functional cure is therefore of urgent need.

Treatment with an oral TLR7 agonist represents a ing solution to provide greater efficacy with better tolerability. Pegylated IFN-α (PEG-IFN-α) is currently used to treat c HBV and is an alternative to ially life-long treatment with antiviral nucleos(t)ide analogues. In a subset of chronic HBV patients, PEG-IFN-α therapy can induce sustained immunologic control of the virus ing a finite duration of y. However, the percentage of HBV patients that achieve seroconversion with interferon therapy is low (up to 27% for HBeAg-positive patients) and the treatment is lly poorly ted. Furthermore, functional cure (defined as HBsAg loss and seroconversion) is also very infrequent with both PEG-IFN-α and nucleos(t)ide treatment. Given these limitations, there is an urgent need for improved therapeutic s to treat and induce a onal cure for chronic HBV. Treatment with an oral, small-molecule TLR7 agonist is a promising approach that has the potential to provide greater efficacy and bility (T. Asselah et al, Clin Liver Dis 2007, 11, 839-849).

In fact, several identified TLR7 agonists have been considered for therapeutic purposes. So far Imiquimod (ALDARATM) is a U.S. FDA approved TLR7 agonist drug for topical use to treat skin lesions by human papillomavirus. The TLR7/8 dual agonist resiquimod (R-848) and the TLR7 agonist 852A have been evaluated for treating human genital herpes and chemotherapy- refractory metastatic melanoma, respectively. ANA773 is an oral pro-drug TLR7 agonist, developed for the treatment of patients with chronic tis C virus (HCV) ion and c hepatitis B infection. GS-9620 is an orally available TLR7 agonist. A phase Ib study demonstrated that treatment with GS-9620 was safe, well tolerated and resulted in dosedependent ISG15 mRNA induction in patients with chronic hepatitis B (E. J. Gane et al, Annu Meet Am Assoc Study Liver Dis (November 1-5, Washington, D.C.) 2013, Abst 946). Therefore there is high unmet clinical need for developing potent and safe TLR7 agonists as new HBV treatment to offer more therapeutic solutions or e existing partly ive treatment.

SUMMARY OF THE INVENTION The present invention es a series of novel 6-aminosulfonimidoylsubstituted tuted-purinone compounds that have Toll-like or agonism activity and their prodrugs. The invention also provides the bio-activity of such compounds to induce SEAP level increase by activating Toll-like receptors, such as TLR7 or, the metabolic conversion of prodrugs to parent compounds in the presence of human hepatocytes, and the therapeutic or lactic use of such compounds and their pharmaceutical compositions comprising these compounds and their gs to treat or prevent infectious disease like HBV or HCV. The present invention also provides compounds with superior activity. In addition, the compounds of formula (I) also show good solubility and PK profiles.

The present invention relates to novel compounds of formula (I), (I), wherein R1 is kyl; R2 is benzyl, said benzyl being unsubstituted or substituted by one, two or three substituents independently selected from halogen and C1-6alkyl; R3 is -NR4R5, wherein R4 is C1-6alkyl or koxyC1-6alkyl; R5 is (C1-6alkyl)2NCOOC1-6alkyl, C1-6alkoxyC1-6alkyl, C1-6alkoxycarbonyl(C1- 6alkyl)aminoC1-6alkyl, C1-6alkoxycarbonyl(phenyl)C1-6alkyl, C1- 6alkoxycarbonylC1-6alkyl, C1-6alkoxycarbonyloxyC1-6alkyl, C1-6alkyl, C1- 6alkylcarbonyl(C1-6alkyl)aminoC1-6alkyl or pyrrolidinylcarbamoyloxyC1- 6alkyl; or R4 and R5 together with the nitrogen they are attached to form a cyclyl; or pharmaceutically acceptable salt, omer or diastereomer thereof; with the proviso that 6-aminobenzyl(propylsulfonimidoyl)(pyrrolidinecarbonyl)purinone; 6-aminobenzyl(piperidinecarbonyl)(propylsulfonimidoyl)purinone; obenzyl(morpholinecarbonyl)(propylsulfonimidoyl)purinone; 6-aminobenzyl(3,3-dimethylpyrrolidinecarbonyl)(propylsulfonimidoyl)purinone; ethyl 1-[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]pyrrolidine carboxylate; 6-amino(2-azaspiro[3.3]heptanecarbonyl)benzyl(propylsulfonimidoyl)purinone; 6-aminobenzyl(2-oxaazaspiro[3.3]heptanecarbonyl)(propylsulfonimidoyl)purin 6-aminobenzyl(3,3-difluoropyrrolidinecarbonyl)(propylsulfonimidoyl)purinone; 6-aminobenzyl(3-fluoromethyl-pyrrolidinecarbonyl)(propylsulfonimidoyl)purin- 8-one; and their omers or diastereomers are excluded.

The invention also relates to their manufacture, medicaments based on a compound in accordance with the invention and their production as well as the use of compounds of formula (I) thereof as TLR7 agonist. Accordingly, the compounds of formula (I) are useful for the treatment or prophylaxis of HBV and/or HCV infection with Toll-like receptors agonism.

DETAILED DESCRIPTION OF THE ION Unless otherwise d, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention s. Furthermore, the following definitions are set forth to illustrate and define the meaning and scope of the various terms used to describe the invention.

DEFINITIONS The term “C1-6alkyl” denotes a saturated, linear or branched chain alkyl group containing 1 to 6, particularly 1 to 4 carbon atoms, for example , ethyl, yl, isopropyl, n-butyl, isobutyl, tert-butyl and the like. ular “C1-6alkyl” groups are methyl, ethyl and yl.

The term “C1-6alkoxy” denotes a group of the formula C1-6alkyl-O-. Examples of C1- 6alkoxy group include, but not limited to, methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, isobutoxy and tert-butoxy. Particular “C1-6alkoxy” groups are methoxy, ethoxy and isopropoxy.

A more particular C1-6alkoxy group is ethoxy.

The term “halogen” and “halo” are used interchangeably herein and denote fluoro, chloro, bromo, or iodo.

The term “heterocyclyl” denotes a monovalent saturated or partly unsaturated mono or bicyclic ring system of 3 to 10 ring atoms, comprising 1 to 5 ring heteroatoms selected from N, O and S, the remaining ring atoms being carbon. In particular embodiments, heterocyclyl is a monovalent saturated monocyclic ring system of 4 to 7 ring atoms, comprising 1, 2, or 3 ring heteroatoms selected from N, O and S, the ing ring atoms being carbon. Examples for monocyclic saturated heterocyclyl are aziridinyl, oxiranyl, azetidinyl, yl, pyrrolidinyl, dimethylpyrrolidinyl, ethoxycarbonylpyrrolidinyl, tetrahydrofuranyl, tetrahydro-thienyl, pyrazolidinyl, imidazolidinyl, idinyl, isoxazolidinyl, thiazolidinyl, dinyl, tetrahydropyranyl, tetrahydrothiopyranyl, piperazinyl, morpholinyl, thiomorpholinyl, dioxothiomorpholinyl, azepanyl, diazepanyl, homopiperazinyl, or oxazepanyl. Monocyclic saturated heterocyclyl can be further substituted by one to three substituents independently ed from halogen, C1-6alkyl and C1-6alkoxycarbonyl. Examples for substituted monocyclic saturated cyclyl are 4-methylpiperazinyl, dimethylpyrrolidinyl, ethoxycarbonylpyrrolidinyl, difluoropyrrolidinyl, fluoro(methyl)pyrrolidinyl. Examples for bicyclic saturated heterocyclyl are azabicyclo[3.2.1]octyl, quinuclidinyl, oxaazabicyclo[3.2.1]octyl, yclo[3.3.1]nonyl, oxaazabicyclo[3.3.1]nonyl, thiaazabicyclo[3.3.1]nonyl, azaspiro[3.3]heptanyl and spiro[3.3]heptanyl. Examples for partly unsaturated heterocyclyl are dihydrofuryl, imidazolinyl, dihydrooxazolyl, tetrahydropyridinyl and dihydropyranyl.

The term “carbonyl” alone or in combination refers to the group -C(O)-.

The term lkylcarbonyl” refers to a group C1-6alkyl-C(O)-, wherein the “C1-6alkyl” is as d above. Particular “C1-6alkylcarbonyl” group is acetyl.

The term “enantiomer” denotes two stereoisomers of a compound which are non- superimposable mirror images of one another.

The term “diastereomer” denotes a stereoisomer with two or more s of chirality and whose molecules are not mirror images of one another. Diastereomers have different physical ties, e.g. melting points, boiling , spectral properties, and reactivities.

The term “pharmaceutically acceptable salts” denotes salts which are not biologically or otherwise undesirable. Pharmaceutically acceptable salts include both acid and base addition salts.

The term “pharmaceutically acceptable acid addition salt” denotes those pharmaceutically acceptable salts formed with inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, carbonic acid, phosphoric acid, and organic acids selected from aliphatic, liphatic, aromatic, araliphatic, heterocyclic, carboxylic, and sulfonic classes of organic acids such as formic acid, acetic acid, propionic acid, glycolic acid, gluconic acid, lactic acid, pyruvic acid, oxalic acid, malic acid, maleic acid, maloneic acid, ic acid, fumaric acid, tartaric acid, citric acid, aspartic acid, ic acid, ic acid, anthranilic acid, benzoic acid, cinnamic acid, mandelic acid, embonic acid, phenylacetic acid, methanesulfonic acid, ethanesulfonic acid, enesulfonic acid, and salicyclic acid.

The term aceutically acceptable base addition salt” denotes those pharmaceutically acceptable salts formed with an organic or inorganic base. Examples of acceptable nic bases include sodium, potassium, ammonium, m, magnesium, iron, zinc, copper, manganese, and aluminum salts. Salts derived from pharmaceutically acceptable organic nontoxic bases includes salts of primary, ary, and tertiary amines, substituted amines including naturally occurring substituted amines, cyclic amines and basic ion exchange resins, such as isopropylamine, trimethylamine, diethylamine, triethylamine, tripropylamine, ethanolamine, 2-diethylaminoethanol, trimethamine, dicyclohexylamine, lysine, arginine, histidine, caffeine, procaine, hydrabamine, choline, betaine, ethylenediamine, glucosamine, methylglucamine, theobromine, purines, piperizine, piperidine, N-ethylpiperidine, and polyamine resins.

Compounds of the general a (I) and their prodrugs which contain one or several chiral centers can either be present as racemates, diastereomeric es, or optically active single isomers. The racemates can be separated according to known methods into the enantiomers. Particularly, diastereomeric salts which can be separated by crystallization are formed from the racemic mixtures by reaction with an optically active acid such as e.g. D- or L- ic acid, mandelic acid, malic acid, lactic acid or camphorsulfonic acid.

The term “prodrug” denotes a form or derivative of a compound which is metabolized in vivo, e.g., by biological fluids or enzymes by a subject after administration, into a pharmacologically active form of the compound in order to produce the desired cological effect. Prodrugs are bed e.g. in “The Organic Chemistry of Drug Design and Drug Action”, by Richard B. Silverman, Academic Press, San Diego, 2004, Chapter 8 Prodrugs and Drug Delivery Systems, pp. 497-558.

“A pharmaceutically active metabolite” is intended to mean a pharmacologically active product ed through metabolism in the body of a specified compound or salt thereof. After entry into the body, most drugs are substrates for al reactions that may change their physical properties and biologic effects. These metabolic conversions, which usually affect the ty of the compounds of the invention, alter the way in which drugs are buted in and ed from the body. However, in some cases, metabolism of a drug is required for therapeutic effect.

The term peutically effective amount” denotes an amount of a compound or molecule of the present invention that, when administered to a subject, (i) treats or prevents the particular disease, condition or disorder, (ii) attenuates, ameliorates or eliminates one or more symptoms of the particular disease, condition, or disorder, or (iii) prevents or delays the onset of one or more symptoms of the particular disease, condition or disorder described . The therapeutically effective amount will vary depending on the compound, the disease state being treated, the ty of the disease treated, the age and ve health of the subject, the route and form of administration, the judgement of the attending medical or veterinary practitioner, and other factors.

The term “pharmaceutical composition” denotes a mixture or solution comprising a therapeutically effective amount of an active pharmaceutical ingredient together with ceutically acceptable excipients to be administered to a mammal, e.g., a human in need thereof.

TLR7 AGONIST AND PRODRUG The present invention relates to a compound of formula (I), wherein R1 is C1-6alkyl; R2 is benzyl, said benzyl being unsubstituted or tuted by one, two or three substituents independently selected from halogen and kyl; R3 is -NR4R5, wherein R4 is C1-6alkyl or koxyC1-6alkyl; R5 is (C1-6alkyl)2NCOOC1-6alkyl, C1-6alkoxyC1-6alkyl, C1-6alkoxycarbonyl(C1- 6alkyl)aminoC1-6alkyl, C1-6alkoxycarbonyl(phenyl)C1-6alkyl, C1- 6alkoxycarbonylC1-6alkyl, koxycarbonyloxyC1-6alkyl, C1-6alkyl, C1- 6alkylcarbonyl(C1-6alkyl)aminoC1-6alkyl or pyrrolidinylcarbamoyloxyC1- 6alkyl; or R4 and R5 together with the nitrogen they are attached to form a heterocyclyl; or pharmaceutically acceptable salt, enantiomer or diastereomer thereof; with the proviso that 6-aminobenzyl(propylsulfonimidoyl)(pyrrolidinecarbonyl)purinone; 6-aminobenzyl(piperidinecarbonyl)(propylsulfonimidoyl)purinone; 6-aminobenzyl(morpholinecarbonyl)(propylsulfonimidoyl)purinone; 6-aminobenzyl(3,3-dimethylpyrrolidinecarbonyl)(propylsulfonimidoyl)purinone; ethyl 1-[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]pyrrolidine ylate; 6-amino(2-azaspiro[3.3]heptanecarbonyl)benzyl(propylsulfonimidoyl)purinone; 6-aminobenzyl(2-oxaazaspiro[3.3]heptanecarbonyl)(propylsulfonimidoyl)purin 6-aminobenzyl(3,3-difluoropyrrolidinecarbonyl)(propylsulfonimidoyl)purinone; 6-aminobenzyl(3-fluoromethyl-pyrrolidinecarbonyl)(propylsulfonimidoyl)purin- 8-one; and their enantiomers or diastereomers are excluded.

A further embodiment of present invention is (ii) a compound of formula (I), wherein R1 is C1-6alkyl; R2 is benzyl, said benzyl being unsubstituted or substituted by halogen or C1-6alkyl; R3 is azetidinyl; piperazinyl substituted by C1-6alkyl; piperidinyl substituted by piperidinyl; pyrrolidinyl; or , wherein R4 is C1-6alkyl or koxyC1-6alkyl; R5 is (C1-6alkyl)2NCOOC1-6alkyl, koxyC1-6alkyl, C1-6alkoxycarbonyl(C1- 6alkyl)aminoC1-6alkyl, C1-6alkoxycarbonyl(phenyl)C1-6alkyl, C1- 6alkoxycarbonylC1-6alkyl, C1-6alkoxycarbonyloxyC1-6alkyl, C1-6alkyl, C1- 6alkylcarbonyl(C1-6alkyl)aminoC1-6alkyl or pyrrolidinylcarbamoyloxyC1- ; or ceutically able salt, enantiomer or diastereomer thereof.

A further embodiment of t invention is (iii) a compound of formula (I), wherein R1 is ethyl or propyl; R2 is benzyl, bromobenzyl, chlorobenzyl, fluorobenzyl or methylbenzyl; R3 is azetidinyl; 4-methylpiperazinyl; piperidinylpiperidinyl; pyrrolidinyl; or -NR4R5, wherein R4 is methyl, ethyl, propyl or methoxyethyl; R5 is acetyl(methyl)aminoethyl, butyl, butyl(methyl)carbamoyloxyethyl, diethylcarbamoyloxyethyl, ethoxycarbonyl(methyl)aminoethyl, ethoxycarbonylethyl, ethoxycarbonylisobutyl, ethoxycarbonylisopentyl, ethoxycarbonylmethyl, ethoxycarbonyloxyethyl, ethoxycarbonyl(phenyl)ethyl, ethyl, isobutyl, isopropoxycarbonylisopentyl, isopropoxycarbonyl(phenyl)ethyl, isopropyl, methoxycarbonyl(methyl)aminoethyl, methoxyethyl, methoxypropyl, propyl, propyl(methyl)carbamoyloxyethyl, pyrrolidinylcarbamoyloxyethyl, tertbutoxycarbonyl l)aminoethyl, tert-butoxycarbonylethyl, tertbutoxycarbonylisopentyl or tert-butoxycarbonyl(phenyl)ethyl; or pharmaceutically acceptable salt, enantiomer or diastereomer f.

A further ment of present invention is ) a compound of formula (I), wherein R1 is ethyl or propyl; R2 is benzyl, benzyl, fluorobenzyl or methylbenzyl; R3 is azetidinyl; 4-methylpiperazinyl; piperidinylpiperidinyl; pyrrolidinyl; or -NR4R5, wherein R4 is methyl, ethyl, propyl or methoxyethyl; R5 is acetyl(methyl)aminoethyl, butyl, butyl(methyl)carbamoyloxyethyl, diethylcarbamoyloxyethyl, ethoxycarbonyl(methyl)aminoethyl, carbonylethyl, ethoxycarbonylisobutyl, ethoxycarbonylisopentyl, ethoxycarbonylmethyl, ethoxycarbonyloxyethyl, ethoxycarbonyl(phenyl)ethyl, ethyl, isobutyl, isopropoxycarbonylisopentyl, isopropoxycarbonyl(phenyl)ethyl, isopropyl, methoxycarbonyl(methyl)aminoethyl, methoxyethyl, methoxypropyl, propyl, propyl(methyl)carbamoyloxyethyl, pyrrolidinylcarbamoyloxyethyl, tertbutoxycarbonyl (methyl)aminoethyl, tert-butoxycarbonylethyl, tertbutoxycarbonylisopentyl or tert-butoxycarbonyl(phenyl)ethyl; or ceutically acceptable salt, enantiomer or diastereomer thereof.

A further embodiment of t invention is (iv) a compound of formula (I), wherein R3 is azetidinyl, 4-methylpiperazinyl, piperidinylpiperidinyl, idinyl, acetyl(methyl)aminoethyl(methyl)amino, bis(methoxyethyl)amino, butyl(ethyl)amino, butyl(methyl)amino, butyl(methyl)carbamoyloxyethyl(methyl)amino, diethylcarbamoyloxyethyl(methyl)amino, ethoxycarbonyl(methyl)aminoethyl(methyl)amino, ethoxycarbonylethyl(methyl)amino, ethoxycarbonylisobutyl(methyl)amino, ethoxycarbonylisopentyl(methyl)amino, ethoxycarbonylmethyl(methyl)amino, carbonyloxyethyl(methyl)amino, ethoxycarbonyl(phenyl)ethyl(methyl)amino, methyl)amino, isobutyl(methyl)amino, isopropoxycarbonylisopentyl(methyl)amino, isopropoxycarbonyl(phenyl)ethyl(methyl)amino, isopropyl(methyl)amino, methoxycarbonyl(methyl)aminoethyl(methyl)amino, methoxyethyl(ethyl)amino, methoxyethyl(methyl)amino, methoxyethyl(propyl)amino, methoxypropyl(methyl)amino, propyl(ethyl)amino, propyl(methyl)amino, propyl(methyl)carbamoyloxyethyl(methyl)amino, idinylcarbamoyloxyethyl(methyl)amino, tertbutoxycarbonyl (methyl)aminoethyl(methyl)amino, tert-butoxycarbonylethyl(methyl)amino, tertbutoxycarbonylisopentyl (methyl)amino or tert-butoxycarbonyl(phenyl)ethyl(methyl)amino; or pharmaceutically acceptable salt, enantiomer or reomer thereof.

A further embodiment of present invention is (v) a compound of formula (I), wherein R1 is ethyl.

A further embodiment of present invention is (vi) a compound of a (I), wherein R2 is benzyl substituted by halogen or C1-6alkyl.

A further embodiment of present invention is (vii) a compound of formula (I), wherein R2 is bromobenzyl, chlorobenzyl, fluorobenzyl or methylbenzyl.

A further embodiment of t invention is (vii-1) a compound of formula (I), wherein R2 is chlorobenzyl, fluorobenzyl or methylbenzyl.

A further embodiment of present invention is (viii) a compound of formula (I), wherein R2 is bromobenzyl, chlorobenzyl or fluorobenzyl.

A further embodiment of t invention is (viii-1) a compound of formula (I), wherein R2 is chlorobenzyl or benzyl.

A further embodiment of present invention is (ix) a compound of formula (I), wherein R3 is - NR4R5, wherein R4 is kyl, R5 is C1-6alkyl.

A further embodiment of present invention is (x) a compound of formula (I), wherein R3 is propyl(methyl)amino or ethyl(methyl)amino.

A r embodiment of present invention is (xi) a compound of formula (I), wherein R1 is C1-6alkyl; R2 is benzyl, said benzyl being substituted by halogen or C1-6alkyl; R3 is -NR4R5, wherein R4 is C1-6alkyl, R5 is C1-6alkyl; or pharmaceutically acceptable salt, enantiomer or diastereomer f.

A further embodiment of present ion is (xii) a compound of formula (I), wherein R1 is ethyl; R2 is methylbenzyl, bromobenzyl, chlorobenzyl or fluorobenzyl; R3 is propyl(methyl)amino or methyl)amino; or pharmaceutically acceptable salt, enantiomer or diastereomer thereof.

A further embodiment of present ion is (xii-1) a compound of formula (I), wherein R1 is ethyl; R2 is methylbenzyl, chlorobenzyl or fluorobenzyl; R3 is (methyl)amino or ethyl(methyl)amino; or pharmaceutically acceptable salt, enantiomer or reomer thereof.

Another ment of present invention is that (xiii) particular compounds of formula (I) are the following: 6-Aminobenzyl-N-methyloxo-N-propyl(propylsulfonimidoyl)purinecarboxamide; 6-Aminobenzyl-N-(2-methoxyethyl)-N-methyloxo(propylsulfonimidoyl)purine carboxamide; 6-Aminobenzyl-N-ethyloxo-N-propyl(propylsulfonimidoyl)purinecarboxamide; 6-Aminobenzyl[4-(1-piperidyl)piperidinecarbonyl](propylsulfonimidoyl)purinone; 6-Aminobenzyl-N-ethyl-N-(2-methoxyethyl)oxo(propylsulfonimidoyl)purine carboxamide; 6-Aminobenzyl-N-butyl-N-ethyloxo(propylsulfonimidoyl)purinecarboxamide; 6-Aminobenzyl-N-(2-methoxyethyl)oxo-N-propyl(propylsulfonimidoyl)purine carboxamide; 6-Aminobenzyl-N,N-bis(2-methoxyethyl)oxo(propylsulfonimidoyl)purine carboxamide; 6-Amino(azetidinecarbonyl)benzyl(propylsulfonimidoyl)purinone; 6-Aminobenzyl-N-isopropyl-N-methyloxo(propylsulfonimidoyl)purinecarboxamide; 6-Aminobenzyl(4-methylpiperazinecarbonyl)(propylsulfonimidoyl)purinone; 6-Aminobenzyl-N-(3-methoxypropyl)-N-methyloxo(propylsulfonimidoyl)purine carboxamide; 6-Aminobenzyl-N-isobutyl-N-methyloxo(propylsulfonimidoyl)purinecarboxamide; Ethyl 2-[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino ]acetate; Ethyl 3-[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino ]propanoate; tert-Butyl 3-[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl- amino]propanoate; Ethyl (2S)[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino ]propanoate; tert-Butyl (2S)[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl- amino]methyl-pentanoate; pyl (2S)[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino ]methyl-pentanoate; Ethyl (2S)[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino ]methyl-butanoate; Ethyl (2S)[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino ]methyl-pentanoate; Ethyl -[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino ]phenyl-propanoate; Isopropyl (2S)[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl- amino]phenyl-propanoate; tert-Butyl (2S)[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl- amino]phenyl-propanoate; N-[2-[Acetyl(methyl)amino]ethyl]aminobenzyl-N-methyloxo (propylsulfonimidoyl)purinecarboxamide; Methyl N-[2-[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino ]ethyl]-N-methyl-carbamate; tert-Butyl N-[2-[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl- amino]ethyl]-N-methyl-carbamate; Ethyl N-[2-[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl- amino]ethyl]-N-methyl-carbamate; 2-[[6-Aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl-amino]ethyl N- butyl-N-methyl-carbamate; 2-[[6-Aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl-amino]ethyl pyrrolidinecarboxylate; 2-[[6-Aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl-amino]ethyl N- methyl-N-propyl-carbamate; 2-[[6-Aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl-amino]ethyl N,N-diethylcarbamate; Aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl-amino]ethyl ethyl ate; 6-Amino-N-butyl[(4-chlorophenyl)methyl]-N-methyloxo[S(S)- propylsulfonimidoyl]purinecarboxamide; 6-amino-N-butyl[(4-chlorophenyl)methyl]-N-methyloxo[S(S)- propylsulfonimidoyl]purinecarboxamide; 6-Amino[(4-chlorophenyl)methyl]-N-ethyl-N-methyloxo(propylsulfonimidoyl)purine carboxamide; 6-Amino-N-methyloxo-N-propyl-2[S(S)-propylsulfonimidoyl](p-tolylmethyl)purine carboxamide; 6-Amino-N-methyloxo-N-propyl-2[S(R)-propylsulfonimidoyl](p-tolylmethyl)purine carboxamide; 6-Amino[S(S)-propylsulfonimidoyl](p-tolylmethyl)(pyrrolidinecarbonyl)purinone; 6-Amino[S(R)-propylsulfonimidoyl](p-tolylmethyl)(pyrrolidinecarbonyl)purinone; 6-Amino-N-(2-methoxyethyl)-N-methyloxo[S(S)-propylsulfonimidoyl](ptolylmethyl )purinecarboxamide; 6-Amino-N-(2-methoxyethyl)-N-methyloxo[S(R)-propylsulfonimidoyl](ptolylmethyl )purinecarboxamide; 6-Amino-N-ethyl-N-methyloxo(propylsulfonimidoyl)(p-tolylmethyl)purine carboxamide; 6-Amino-N-butyl-N-methyloxo(propylsulfonimidoyl)(p-tolylmethyl)purine carboxamide; 6-Amino[(4-chlorophenyl)methyl][S(R)-ethylsulfonimidoyl]-N-methyloxo-N-propyl- purinecarboxamide; 6-Amino[(4-chlorophenyl)methyl][S(S)-ethylsulfonimidoyl]-N-methyloxo-N-propylpurinecarboxamide 6-Amino[(4-chlorophenyl)methyl]-N-ethyl-2[S(S)-ethylsulfonimidoyl]-N-methyloxopurinecarboxamide 6-Amino[(4-chlorophenyl)methyl]-N-ethyl[S(R)-ethylsulfonimidoyl]-N-methyloxopurinecarboxamide 6-Amino[S(S)-ethylsulfonimidoyl]-N-methyloxo-N-propyl(p-tolylmethyl)purine carboxamide; 6-Amino[S(R)-ethylsulfonimidoyl]-N-methyloxo-N-propyl(p-tolylmethyl)purine carboxamide; 6-Amino-N-ethyl-2[S(S)-ethylsulfonimidoyl]-N-methyloxo(p-tolylmethyl)purine carboxamide; 6-Amino-N-ethyl[S(R)-ethylsulfonimidoyl]-N-methyloxo(p-tolylmethyl)purine carboxamide; o[S(S)ethylsulfonimidoyl][(4-fluorophenyl)methyl]-N-methyloxo-N-propylpurinecarboxamide 6-Amino[S(R)ethylsulfonimidoyl][(4-fluorophenyl)methyl]-N-methyloxo-N-propylpurinecarboxamide 6-Amino-N-ethyl(ethylsulfonimidoyl)[(4-fluorophenyl)methyl]-N-methyloxo-purine carboxamide; 6-Amino-N-ethyl[S(S)-(ethylsulfonimidoyl)][(4-fluorophenyl)methyl]-N-methyloxo- purinecarboxamide; 6-Amino-N-ethyl[S(R)-(ethylsulfonimidoyl)][(4-fluorophenyl)methyl]-N-methyloxopurinecarboxamide 6-Amino[(4-bromophenyl)methyl](ethylsulfonimidoyl)-N-methyloxo-N-propyl-purine- 7-carboxamide; 6-Amino[S(R)-ethylsulfonimidoyl][(4-bromophenyl)methyl]-N-methyloxo-N-propylpurinecarboxamide o[S(S)-ethylsulfonimidoyl][(4-bromophenyl)methyl]-N-methyloxo-N-propylpurinecarboxamide 6-Amino[(4-bromophenyl)methyl]-N-ethyl(ethylsulfonimidoyl)-N-methyloxo-purine carboxamide; 6-Amino[(4-bromophenyl)methyl]-N-ethyl[S(S)-(ethylsulfonimidoyl)]-N-methyloxopurinecarboxamide ; and 6-Amino[(4-bromophenyl)methyl]-N-ethyl[S(R)-(ethylsulfonimidoyl)]-N-methyloxopurinecarboxamide or ceutically acceptable salt, enantiomer or diastereomer thereof.

Another ment of present invention is that (xiv) more particular compounds of formula (I) are the following: 6-Aminobenzyl-N-methyloxo-N-propyl(propylsulfonimidoyl)purinecarboxamide; 6-Amino[(4-chlorophenyl)methyl][S(R)-ethylsulfonimidoyl]-N-methyloxo-N-propylpurinecarboxamide 6-Amino[(4-chlorophenyl)methyl][S(S)-ethylsulfonimidoyl]-N-methyloxo-N-propyl- purinecarboxamide; 6-Amino[(4-chlorophenyl)methyl]-N-ethyl-2[S(S)-ethylsulfonimidoyl]-N-methyloxopurinecarboxamide 6-Amino[(4-chlorophenyl)methyl]-N-ethyl[S(R)-ethylsulfonimidoyl]-N-methyloxopurinecarboxamide 6-Amino[S(S)-ethylsulfonimidoyl]-N-methyloxo-N-propyl(p-tolylmethyl)purine carboxamide; 6-Amino[S(R)-ethylsulfonimidoyl]-N-methyloxo-N-propyl(p-tolylmethyl)purine amide; 6-Amino-N-ethyl-2[S(S)-ethylsulfonimidoyl]-N-methyloxo(p-tolylmethyl)purine carboxamide; 6-Amino-N-ethyl[S(R)-ethylsulfonimidoyl]-N-methyloxo(p-tolylmethyl)purine carboxamide; 6-amino(ethylsulfonimidoyl)[(4-fluorophenyl)methyl]-N-methyloxo-N-propyl-purine carboxamide; 6-Amino[S(S)ethylsulfonimidoyl][(4-fluorophenyl)methyl]-N-methyloxo-N-propylpurinecarboxamide 6-Amino[S(R)ethylsulfonimidoyl][(4-fluorophenyl)methyl]-N-methyloxo-N-propylpurinecarboxamide 6-Amino-N-ethyl(ethylsulfonimidoyl)[(4-fluorophenyl)methyl]-N-methyloxo-purine carboxamide; 6-Amino-N-ethyl[S(S)-(ethylsulfonimidoyl)][(4-fluorophenyl)methyl]-N-methyloxopurinecarboxamide 6-Amino-N-ethyl[S(R)-(ethylsulfonimidoyl)][(4-fluorophenyl)methyl]-N-methyloxopurinecarboxamide 6-Amino[(4-bromophenyl)methyl](ethylsulfonimidoyl)-N-methyloxo-N-propyl-purine- 7-carboxamide; 6-Amino[S(R)-ethylsulfonimidoyl][(4-bromophenyl)methyl]-N-methyloxo-N-propylpurinecarboxamide o[S(S)-ethylsulfonimidoyl][(4-bromophenyl)methyl]-N-methyloxo-N-propylpurinecarboxamide 6-Amino[(4-bromophenyl)methyl]-N-ethyl(ethylsulfonimidoyl)-N-methyloxo-purine carboxamide; 6-Amino[(4-bromophenyl)methyl]-N-ethyl[S(S)-(ethylsulfonimidoyl)]-N-methyloxopurinecarboxamide ; and 6-Amino[(4-bromophenyl)methyl]-N-ethyl[S(R)-(ethylsulfonimidoyl)]-N-methyloxopurinecarboxamide or pharmaceutically acceptable salt, enantiomer or diastereomer thereof.

In some embodiments, nds of present ion were tested and compared with the following reference compounds. As the most successful biopharmaceutical companies focusing on discovery and development of TLR7 agonists for treating liver diseases, Gilead has the most advanced TLR7 agonist pipeline with leading compounds such as GS-9620 which has entered into Phase II studies. Gilead compound GS-9620 disclosed in US20100143301 as example 49, compound S-2 and compound S-3 disclosed in JP1999193282 were all chosen as the reference compounds in this application: N O O N N (GS-9620), (S-2), (S-3).

SYNTHESIS The compounds of the t invention can be prepared by any conventional means.

Suitable processes for synthesizing these compounds as well as their starting materials are provided in the schemes below and in the examples. All tuents, in particular, R1 to R14 are as defined above unless otherwise indicated. Furthermore, and unless explicitly otherwise stated, all reactions, reaction conditions, abbreviations and symbols have the meanings well known to a person of ordinary skill in organic chemistry.

Scheme 1 N C N N H 2 O N R C N + NH2 H2N O VII VI NH2 NH2 H H 1 H N R X N N N N N O O O O S N N HS N N S N 2 2 R 2 R R 1 R V IV III O 3 NH2 R H N N N N NH O NH O O N N S N N S R 1 R 1 R II I A compound of formula VI is prepared by cyclization of isocyanate VII with aminomalononitrile p-toluenesulfonate. Then e V is synthesized by reaction of compound of a VI with benzoyl isothiocyanate in the presence of nic base, such as NaOH or KOH. Alkylation of bicycle V with alkylhalide in the presence of base, such as K2CO3, NaH or Cs2CO3, gives compound of formula IV. Compound of a III is prepared by oxidation of nd of a IV with an oxidant, such as hloroperoxybenzoic acid, ureahydrogen peroxide adduct and HIO4. Compound of a II is obtained by imination of compound of formula III with imination reagent, such as sodium azide in acid, said acid is, for example, Eaton’s reagent or PPA. Compound of formula I is obtained by reaction of compound of formula II with carbamoyl chloride in the presence of a mixed base such as ne and triethylamine, pyridine and DIPEA, DMAP and triethylamine, or DMAP and DIPEA.

Scheme 2 CF COOH PMBNH 3 2 IV VIII Compound of formula II can also be prepared as Scheme 2.

A compound of formula X is prepared by reaction of compound of formula XI with R2NH2.

Reduction of compound X with reducing reagent, such as Zinc or Iron powder in AcOH, gives the nd of formula IX. Cyclization of compound of formula IX with cyclization ts, such as phosgene, carbonyl diimidazole, diethyl carbonate and triphosgene, affords compound of formula VIII. A compound of formula IVa is prepared by treating the compound of formula VIII with PMBNH2. A compound of formula III is prepared by deprotection of nd of a IVa with acid, such as CF3COOH, followed by oxidation with an oxidant, such as metachloroperoxybenzoic acid, urea-hydrogen peroxide adduct and HIO4. Compound of formula II is obtained by the imination of compound of formula III with imination reagent, such as sodium azide in acid, said acid is for example Eaton’s reagent or PPA.

This invention also s to a process for the preparation of a compound of formula (I) sing the reaction of: the reaction of a compound of formula (II), NH O O N S N 1 R R (II), with oyl de in the presence of a mixed base; wherein R1 and R2 are defined above.

In above step, the mixed base can be, for example, pyridine and triethylamine, pyridine and DIPEA, DMAP and triethylamine, or DMAP and DIPEA.

A compound of formula (I) when manufactured ing to the above process is also an object of the invention.

PHARMACEUTICAL COMPOSITIONS AND ADMINISTRATION Another embodiment provides pharmaceutical compositions or medicaments ning the compounds of the invention and a therapeutically inert carrier, diluent or excipient, as well as methods of using the compounds of the invention to prepare such compositions and medicaments.

In one example, compounds of formula (I) may be ated by mixing at ambient ature at the appropriate pH, and at the desired degree of purity, with physiologically acceptable carriers, i.e., carriers that are non-toxic to recipients at the dosages and concentrations employed into a galenical administration form. The pH of the formulation depends mainly on the particular use and the concentration of compound, but preferably ranges anywhere from about 3 to about 8.

In one example, a compound of formula (I) are formulated in an e buffer, at pH 5. In another embodiment, the compounds of formula (I) are sterile. The compound may be stored, for example, as a solid or amorphous composition, as a lyophilized formulation or as an aqueous solution.

Compositions are formulated, dosed, and administered in a fashion consistent with good medical practice. Factors for consideration in this context include the particular disorder being d, the particular mammal being treated, the clinical condition of the dual patient, the cause of the disorder, the site of delivery of the agent, the method of administration, the scheduling of administration, and other factors known to medical tioners. The “effective amount” of the compound to be stered will be governed by such considerations, and is the minimum amount necessary to activate TLR7 receptor and lead to produce INF-α and other cytokines, which can be used, but not limited, for the treatment or prevention of tis B and/or C viral infected patients.

In one example, the pharmaceutically effective amount of the compound of the invention administered erally per dose will be in the range of about 0.1 to 50 mg/kg, alternatively about 0.1 to 30 mg/kg of patient body weight per day, with the typical initial range of nd used being 0.3 to 15 mg/kg/day. In another embodiment, oral unit dosage forms, such as tablets and capsules, preferably contain from about 20 to about 1000 mg of the compound of the invention.

The compounds of the invention may be administered by any suitable means, including oral, topical (including buccal and sublingual), rectal, vaginal, transdermal, parenteral, subcutaneous, intraperitoneal, intrapulmonary, intradermal, intrathecal and epidural and intranasal, and, if desired for local treatment, esional administration. Parenteral infusions include uscular, intravenous, intraarterial, intraperitoneal, or aneous administration.

The compounds of the present invention may be administered in any convenient strative form, e.g., s, s, capsules, solutions, dispersions, suspensions, syrups, sprays, suppositories, gels, emulsions, patches, etc. Such compositions may contain components conventional in pharmaceutical preparations, e.g., diluents, carriers, pH modifiers, sweeteners, bulking agents, and further active agents.

A typical formulation is prepared by mixing a compound of the present invention and a carrier or excipient. le carriers and excipients are well known to those skilled in the art and are described in detail in, e.g., Ansel, Howard C., et al., Ansel’s Pharmaceutical Dosage Forms and Drug Delivery Systems. Philadelphia: Lippincott, ms & Wilkins, 2004; Gennaro, Alfonso R., et al. Remington: The Science and Practice of Pharmacy. Philadelphia: Lippincott, Williams & Wilkins, 2000; and Rowe, Raymond C. Handbook of Pharmaceutical Excipients.

Chicago, Pharmaceutical Press, 2005. The ations may also include one or more buffers, stabilizing , surfactants, wetting agents, lubricating agents, emulsifiers, suspending agents, preservatives, antioxidants, opaquing agents, glidants, processing aids, colorants, sweeteners, perfuming agents, flavoring agents, diluents and other known additives to provide an elegant presentation of the drug (i.e., a compound of the t invention or pharmaceutical composition thereof) or aid in the manufacturing of the pharmaceutical product (i.e., medicament).

An example of a suitable oral dosage form is a tablet ning about 20 to 1000 mg of the compound of the invention compounded with about 30 to 90 mg anhydrous lactose, about 5 to 40 mg sodium croscarmellose, about 5 to 30 mg polyvinylpyrrolidone (PVP) K30, and about 1 to 10 mg ium stearate. The powdered ingredients are first mixed together and then mixed with a solution of the PVP. The resulting composition can be dried, granulated, mixed with the magnesium te and compressed to tablet form using conventional equipment. An example of an aerosol formulation can be prepared by dissolving the compound, for example 20 to 1000 mg, of the ion in a suitable buffer on, e.g. a phosphate buffer, adding a tonicifier, e.g. a salt such sodium chloride, if desired. The solution may be filtered, e.g., using a 0.2 micron filter, to remove impurities and contaminants.

An embodiment, therefore, includes a ceutical composition sing a compound of formula (I) or pharmaceutically acceptable salts or enantiomers or diastereomers thereof.

In a further embodiment includes a pharmaceutical composition comprising a compound of formula (I) or pharmaceutically acceptable salts or enantiomers or diastereomers thereof, together with a pharmaceutically acceptable carrier or excipient. r embodiment includes a ceutical composition sing a compound of formula (I) or pharmaceutically acceptable salts or enantiomers or diastereomers thereof for use in the ent of hepatitis B virus infection.

INDICATIONS AND METHODS OF TREATMENT The present invention provides methods for treating or preventing a tis B viral infection and/or hepatitis C viral infection in a patient in need thereof.

The present invention further provides methods for introducing a eutically effective amount of a compound of formula (I) or other compounds of the invention into the blood stream of a patient for the treatment and/or prevention of hepatitis B and/or C viral infection.

The methods of the present invention are particularly well suited for human patients. In particular, the methods and doses of the present invention can be useful for, but not limited to, HBV and/or HCV infected patients. The methods and doses of the present invention are also useful for patients undergoing other antiviral ents. The prevention methods of the present ion are particularly useful for patients at risk of viral infection. These patients include, but are not limited to health care workers, e.g., doctors, nurses, hospice care givers; military personnel; teachers; childcare workers; patients ing to, or living in, foreign locales, in particular third world s including social aid workers, missionaries, and foreign diplomats.

Finally, the methods and compositions include the treatment of tory patients or patients ant to treatment such as resistance to reverse transcriptase inhibitors, protease inhibitors, etc.

Another embodiment includes a method of treating or preventing tis B viral infection and/or hepatitis C viral infection in a mammal in need of such treatment, wherein the method comprises administering to said mammal a therapeutically ive amount of a nd of formula (I) or enantiomers, diastereomers, prodrugs or pharmaceutically able salts thereof.

BRIEF DESCRIPTION OF THE FIGURES Figure 1 Single crystal X-ray diffraction of Example 41-B.

Figure 2 Single crystal X-ray diffraction of Example 42-A.

Figure 3 Single crystal X-ray diffraction of Example 43-B.

Figure 4 shows the HBV DNA, HBsAg, and anti-HBs antibody level of the V infected mice treated with Vehicle, Example 43-A at 10 mg/kg QOD and QW for 42 days. The results are presented as mean ± SEM. LLOQ: lower limit of quantification.

Figure 5 shows the HBV DNA, HBsAg, and anti-HBs antibody levels of AAV-HBV infected mice treated with Vehicle, Example 41-A at 1, 3, 10 mg/kg QOD, and 10 mg/kg QW for 42 days.

The s are presented as mean ± SEM. LLOQ: lower limit of fication.

Figure 6 shows the HBV DNA, HBsAg, and anti-HBs antibody levels of AAV-HBV infected mice treated with Vehicle, Example 42-A at 1, 3, and 10 mg/kg QOD for 42 days. The results are presented as mean ± SEM. LLOQ: lower limit of quantification.

Figure 7 shows the HBV DNA, HBsAg, and Bs antibody levels of AAV-HBV infected mice treated with Vehicle, Example 41-B at 1, 3, and 10 mg/kg QOD for 42 days. The results are presented as mean ± SEM. LLOQ: lower limit of fication.

EXAMPLES The ion will be more fully understood by reference to the following examples. They should not, however, be construed as limiting the scope of the invention.

ABBREVIATIONS aq. aqueous BSA: N, O-bis(trimethylsilyl)acetamide CDI: N,N’-carbonyl diimidazole DIEPA: N, N-diethylpropylamine DBU: 1,8-Diazabicycloundecene DPPA: diphenylphosphoryl azide EC50: the molar concentration of an agonist, which prod uces 50% of the maximum le response for that agonist.

EDC: N1-((ethylimino)methylene)-N3,N3-dimethylpropane-1,3-diamine EtOAc or EA: ethyl acetate HATU: (1-[Bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5- b]pyridinium 3-oxid hexafluorophosphate) hr(s): hour(s) HPLC: high performance liquid chromatography HOBt: N-hydroxybenzotriazole MS (ESI): mass spectroscopy (electron spray ionization) m-CPBA: roperbenzoic acid MTEB: methyl tert-butyl ether NMP: N-methylpyrrolidone obsd. observed PE: petroleum ether PMB: p-methoxybenzyl PPA: polyphosphoric acid QOD every other day QW once a week RT or rt: room temperature sat. saturated TFA: trifluoroacetic acid TEA: triethylamine V/V volume ratio L EXPERIMENTAL CONDITIONS Intermediates and final compounds were purified by flash tography using one of the following instruments: i) Biotage SP1 system and the Quad 12/25 Cartridge module. ii) ISCO combi-flash chromatography instrument. Silica gel Brand and pore size: i) KP-SIL 60 Å, particle size: 40-60 µm; ii) CAS registry NO: Silica Gel: 632314, particle size: 47-60 micron silica gel; iii) ZCX from Qingdao Haiyang Chemical Co., Ltd, pore: 200-300 or 300-400.

Intermediates and final compounds were purified by ative HPLC on reversed phase column using X BridgeTM Perp C18 (5 µm, OBDTM 30 × 100 mm) column or SunFireTM Perp C18 (5 µm, OBDTM 30 × 100 mm) column.

LC/MS spectra were obtained using a Waters UPLC-SQD Mass. Standard LC/MS ions were as follows (running time 3 minutes): Acidic condition: A: 0.1% formic acid and 1% acetonitrile in H2O; B: 0.1% formic acid in acetonitrile; Basic condition: A: 0.05% NH3·H2O in H2O; B: acetonitrile.

Mass a (MS): generally only ions which indicate the parent mass are reported, and unless otherwise stated the mass ion quoted is the positive mass ion (M+H)+.

NMR Spectra were obtained using Bruker Avance 400MHz.

All reactions involving air-sensitive reagents were performed under an argon atmosphere.

Reagents were used as received from cial suppliers without further purification unless otherwise noted.

PREPARATIVE EXAMPLES Preparation of ediate Intermediate AA N-methyl-N-propyl-carbamoyl chloride AA To a mixture of N-methylpropanamine (5 g, 68.4 mmol) and sodium hydrogencarbonate (11.5 g, 137 mmol) in DCM (70 mL) at 0 oC was added bis(trichloromethyl) carbonate (8.11 g, 27.3 mmol) in DCM (30 mL) dropwise. The mixture was d at room temperature for 2 hrs and filtered. The filtrate was concentrated in vacuo. The obtained yl-N-propyl-carbamoyl chloride (7.2 g, Intermediate AA) was used for next step without further cation.

Intermediate AB N-(2-Methoxyethyl)-N-methyl-carbamoyl chloride Intermediate AB was prepared in analogy to Intermediate AA by using 2-methoxy-N- methyl-ethanamine instead of N-methylpropanamine. N-(2-Methoxyethyl)-N-methylcarbamoyl chloride (8 g, Intermediate AB) was obtained and used for next step without further purification.

Intermediate AC N-Ethyl-N-propyl-carbamoyl chloride AC Intermediate AC was prepared in analogy to Intermediate AA by using N-ethylpropan- e instead of N-methylpropanamine. N-Ethyl-N-propyl-carbamoyl chloride (12.6 g, Intermediate AC) was obtained as a yellow oil and used for next step without further cation.

Intermediate AD N-Ethyl-N-(2-methoxyethyl)carbamoyl chloride Intermediate AD was prepared in y to Intermediate AA by using N-ethyl methoxyethanamine instead of N-methylpropanamine. The crude N-ethyl-N-(2- methoxyethyl)carbamoyl chloride (2.5 g, ediate AD) was obtained as a light yellow oil and used for next step without further purification.

Intermediate AE N-Butyl-N-ethyl-carbamoyl chloride Intermediate AE was prepared in analogy to Intermediate AA by using N-ethylbutan amine (5 g) instead of N-methylpropanamine. The crude l-N-ethyl-carbamoyl chloride (6.3 g, Intermediate AE) was obtained as a light yellow oil and used for next step without further purification.

Intermediate AF N-(2-Methoxyethyl)-N-propyl-carbamoyl chloride Intermediate AF was prepared in analogy to Intermediate AA by using N-(2- methoxyethyl)propanamine (2 g, 17.1 mmol) instead of N-methylpropanamine. The crude N-(2-methoxyethyl)-N-propyl-carbamoyl chloride (2.5 g, Intermediate AF) was obtained as a light yellow oil and used for next step without r cation. ediate AG N,N-Bis(2-methoxyethyl)carbamoyl chloride Intermediate AG was prepared in analogy to Intermediate AA by using of bis(2- methoxyethyl)amine (2 g, 15 mmol) instead of N-methylpropanamine. The crude product N,N-bis(2-methoxyethyl)carbamoyl chloride (2.6 g, Intermediate AG) was obtained as a light yellow oil and used for next step without further purification.

Intermediate AH Azetidinecarbonyl chloride ediate AH was prepared in analogy to Intermediate AA by using azetidine hydrochloride (10.7 g, 107 mmol) and sodium bicarbonate (3 equiv.) instead of N-methylpropan- 1-amine and sodium bicarbonate (2 equiv.). The crude azetidinecarbonyl chloride (1.5 g, Intermediate AH) was obtained as a light yellow oil and used for next step t further purification.

Intermediate AI N-Isopropyl-N-methyl-carbamoyl chloride Intermediate AI was prepared in analogy to Intermediate AA by using N-methylpropan- 2-amine (5 g, 19.4 mmol) instead of N-methylpropanamine. The crude N-isopropyl-N-methylcarbamoyl chloride (8.6 g, Intermediate AI) was ed as a yellow oil and used for next step without further purification.

Intermediate AL utyl-N-methyl-carbamoyl chloride AL Intermediate AL was prepared in analogy to Intermediate AA by using N dimethylpropanamine (4.8 g) instead of N-methylpropanamine. The crude N-isobutyl-N- methyl-carbamoyl chloride (8.1 g, Intermediate AL) was obtained as a light yellow oil and used for next step without further cation.

Intermediate AP Ethyl 2-[chlorocarbonyl(methyl)amino]acetate To a solution of triphosgene (728 mg, 2.45 mmol) in DCM (5 mL) was added a solution of ethyl 2-(methylamino)acetate hydrochloride (1.3 g, 8.46 mmol) and pyridine (1 mL) in DCM (5 mL) se at 0oC. The reaction mixture became orange and a yellow precipitate appeared, then it was allowed to warm to room temperature. After stirred for 1 hr, aqueous HCl (0.1N, 25 mL) was added to the reaction mixture, the organic layer was separated, washed with 0.1 N HCl (10 mL) twice, brine (10 mL), dried over Na2SO4 and concentrated in vacuo to give the crude ethyl 2-[chlorocarbonyl(methyl)amino]acetate (2.0 g, ediate AP) as a light yellow oil and used for next step without further purification.

Intermediate AR tert-Butyl 3-[chlorocarbonyl(methyl)amino]propanoate Step 1: Preparation of utyl 3-(methylamino)propanoate (Compound AR-1) AR-1 To a solution of tert-butyl acrylate (3 g) in DMF (40 mL) was added methylamine hydrochloride (4.74 g, 70 mmol) and DBU (21.4 g, 140 mmol) at -45oC. Then the reaction temperature was allowed to warm to -10 oC. The reaction mixture was stirred at the same temperature for 2.5 hrs. Et2O (200 mL) was added and the resulting mixture was washed with brine (50 mL) four times. The separated organic layer was dried over Na2SO4 and concentrated in vacuo to afford tert-butyl 3-(methylamino)propanoate (3.5 g, Compound AR-1) as a light yellow oil.

Step 2: ation of tert-butyl 3-[chlorocarbonyl(methyl)amino]propanoate (Intermediate AR) Intermediate AR was prepared in analogy to Intermediate AP by using tert-butyl 3- (methylamino)propanoate (3.4 g, Compound AR-1) instead of ethyl 2-(methylamino)acetate hydrochloride. The crude tert-butyl 3-[chlorocarbonyl(methyl)amino]propanoate (3.5 g, Intermediate AR) was obtained and used for next step without further purification.

Intermediate AS Ethyl -[chlorocarbonyl(methyl)amino]propanoate Step 1: Preparation of ethyl (2S)(methylamino)propanoate hydrochloride und AS-1) HN HCl To a solution of (2S)(methylamino)propanoic acid (1 g, 9.70 mmol) in EtOH (10 mL) was added SOCl2 (1.50 g, 12.61 mmol) dropwise at 0 oC in 0.5 hr. The reaction mixture was stirred at 25 oC for 15.5 hrs, then diluted with EA (20 mL), washed with H2O (5 mL) and brine (5 mL). The c layer was dried over Na2SO4 and concentrated in vacuo. Ethyl (2S) (methylamino)propanoate hydrochloride (1.8 g, Compound AS-1) was obtained as a yellow oil and used for next step without further purification.

Step 2: ation of ethyl (2S)(methylamino)propanoate (Compound AS-2) A solution of ethyl (2S)(methylamino)propanoate hydrochloride (1.8 g, nd AS- 1) in EA (10 mL) was adjusted to pH = 8 with 10 wt. % aqueous NaHCO3. The reaction mixture was stirred at room temperature for 0.5 hr. The organic layer was washed with brine (5 mL), dried over Na2SO4 and concentrated in vacuo. Ethyl (2S)(methylamino)propanoate (620 mg, nd AS-2) was obtained as a yellow oil and used for the next step without further purification.

Step 3: ation of ethyl (2S)[chlorocarbonyl(methyl)amino]propanoate (Intermediate AS) Intermediate AS was prepared in analogy to Intermediate AP by using ethyl (2S) (methylamino)propanoate (260 mg, Compound AS-2) instead of ethyl 2-(methylamino)acetate hydrochloride. The crude ethyl (2S)[chlorocarbonyl(methyl)amino]propanoate (200 mg, Intermediate AS) was obtained as a yellow oil and used for the next step without further purification.

Intermediate AT tert-Butyl (2S)[chlorocarbonyl(methyl)amino]methyl-pentanoate Step 1: Preparation of tert-butyl (2S)methyl(methylamino)pentanoate (Compound AT-1) AT-1 ylpropene (25 g, 446 mmol) was bubbled into DCM (50 mL) at -78°C. Then the 2- methylpropene solution was added to a solution of (S)methyl(methylamino)pentanoic acid hydrochloride (500 mg, 2.75 mmol) and H2SO4 (3.68 g, 2 mL, 37.5 mmol) in dioxane (20 mL) at 0°C. The reaction mixture was stirred at room temperature for 18 hrs in a sealed tube. The reaction solution was poured into an ice cold s KOH solution (8.4 g in water (30mL)) and the resulting mixture was extracted with DCM (50 mL) twice. The combined organic layer was washed with brine (30 mL) twice, dried over Na2SO4 and trated in vacuo to afford the crude product tert-butyl (2S)methyl(methylamino)pentanoate (Compound AT-1) as a light yellow oil.

Step 2: Preparation of tert-butyl (2S)[chlorocarbonyl(methyl)amino]methyl- pentanoate (Intermediate AT) Intermediate AT was prepared in analogy to Intermediate AP by using tert-butyl (2S) methyl(methylamino)pentanoate (300 mg, Compound AT-1) instead of ethyl 2- (methylamino)acetate hydrochloride. The crude tert-butyl (2S) [chlorocarbonyl(methyl)amino]methyl-pentanoate (350 mg, Intermediate AT) was obtained as a light yellow oil and used for the next step without further purification.

Intermediate AU Isopropyl (2S)[chlorocarbonyl(methyl)amino]methyl-pentanoate N O Step 1: ation of isopropyl (2S)methyl(methylamino)pentanoate hydrochloride (Compound AU-1) To a solution of (S)methyl(methylamino)pentanoic acid hydrochloride (0.5 g) in i- PrOH (7.8 g, 10 mL) was added thionyl chloride (655 mg, 402 µL) se at room temperature. The resulting mixture was stirred and refluxed for 16 hrs and then concentrated in vacuo. The residue was basified with saturated aqueous NaHCO3 (30 mL) and extracted with DCM (50 mL). The organic layer was washed with brine, dried over Na2SO4 and trated in vacuo. The residue was ed with HCl/EtOAc (10 mL, 1 mmol/mL) and concentrated to afford isopropyl (2S)methyl(methylamino)pentanoate hloride (510 mg, Compound AU-1) as a white solid.

Step 2: Preparation of isopropyl (2S)[chlorocarbonyl(methyl)amino]methyl- pentanoate (Intermediate AU) N O Intermediate AU was prepared in analogy to Intermediate AP by using pyl - methyl(methylamino)pentanoate hydrochloride (500 mg, Compound AU-1) instead of ethyl 2-(methylamino)acetate hloride. The crude isopropyl (2S) [chlorocarbonyl(methyl)amino]methyl-pentanoate (650 mg, Intermediate AU) was obtained as a light yellow oil and used for the next step without further purification.

Intermediate AV Ethyl (2S)[chlorocarbonyl(methyl)amino]methyl-butanoate N O AV Step 1: Preparation of ethyl -methyl(methylamino)butanoate hydrochloride (Compound AV-1) To a solution of (2S)methyl(methylamino)butanoic acid (1.0 g, 7.6 mmol) in EtOH (10 mL) was added thionyl chloride (2.45 g, 21 mmol) dropwise at room temperature. The resulting mixture was stirred and refluxed for 16 hrs and then concentrated in vacuo. The residue was basified with saturated aqueous NaHCO3 (30 mL) and extracted with DCM (50 mL) twice.

The combined organic layer was washed with brine, dried over Na2SO4 and concentrated in vacuo. The residue was dissolved in HCl/EtOAc (10 mL, 1 M) and concentrated to afford ethyl (2S)methyl(methylamino)butanoate hydrochloride (1.9 g, Compound AV-1) as a white solid.

Step 2: Preparation of ethyl (2S)[chlorocarbonyl(methyl)amino]methyl-butanoate (Intermediate AV) N O ediate AV was prepared in analogy to Intermediate AP by using ethyl (2S) (methylamino)butanoate hydrochloride (500 mg, Compound AV-1) d of ethyl 2- (methylamino)acetate hydrochloride. The crude ethyl (2S)[chlorocarbonyl(methyl)amino] methyl-butanoate (600 mg, Intermediate AV) was obtained as a light yellow oil and used for the next step without further purification.

Intermediate AW Ethyl (2S)[chlorocarbonyl(methyl)amino]methyl-pentanoate N O AW Step 1: Preparation of ethyl (2S)methyl(methylamino)pentanoate hydrochloride (Compound AW-1) HN O To a solution of (2S)methyl(methylamino)pentanoic acid (1 g, 6.9 mmol) in EtOH (10 mL) was added thionyl chloride (1.07 g, 8.3 mmol) dropwise at room temperature. The resulting mixture was stirred at reflux for 16 hrs and then concentrated in vacuo. The residue was basified with saturated aqueous NaHCO3 (30 mL) and ted with DCM (50 mL). The organic layer was washed with brine, dried over Na2SO4 and concentrated in vacuo. The residue was salified with HCl/EtOAc (10 mL, 1mmol/mL) and concentrated to give ethyl (2S)methyl- 2-(methylamino)pentanoate hloride (1.8 g, Compound AW-1) as a white solid.

Step 2: Preparation of ethyl (2S)[chlorocarbonyl(methyl)amino]methyl-pentanoate mediate AW) N O Intermediate AW was prepared in analogy to Intermediate AP by using ethyl (2S) methyl(methylamino)pentanoate hloride (610 mg, AW-1) instead of ethyl 2- (methylamino)acetate hydrochloride. The crude ethyl (2S)[chlorocarbonyl(methyl)amino] methyl-pentanoate (280 mg, Intermediate AW) was obtained as a light yellow oil and used for the next step without further cation.

Intermediate AX Ethyl (2S)[chlorocarbonyl(methyl)amino]phenyl-propanoate ediate AX was prepared in analogy to Intermediate AP by using (S)-ethyl (methylamino)phenylpropanoate instead of ethyl 2-(methylamino)acetate hydrochloride. The crude ethyl (2S)[chlorocarbonyl(methyl)amino]phenyl-propanoate (200 mg, Intermediate AX) was obtained as a light yellow oil and used for the next step without further purification Intermediate AY Isopropyl -[chlorocarbonyl(methyl)amino]phenyl-propanoate N O Intermediate AY was prepared in analogy to Intermediate AP by using pyl (2S) (methylamino)phenyl-propanoate (190 mg) instead of ethyl 2-(methylamino)acetate hydrochloride. The crude isopropyl (2S)[chlorocarbonyl(methyl)amino]phenyl-propanoate (220 mg, Intermediate AY) was obtained as light brown oil and used for the next step without further purification.

Intermediate AZ (S)-tert-butyl 2-((chlorocarbonyl)(methyl)amino)phenylpropanoate N O Step 1: Preparation of tert-butyl -(methylamino)phenyl-propanoate (Compound AZ-1) 2-Methylpropene (25 g, 446 mmol) was bubbled into DCM (50 mL) at -78 oC. Then the 2- methylpropene solution was added to a on of (S)(methylamino)phenylpropanoic acid (500 mg) and H2SO4 (3.68 g, 2 mL) in dioxane (20 mL) at 0 oC. The reaction e was stirred at room temperature for 18 hrs in a sealed tube. The reaction mixture was poured into an ice cold aqueous KOH solution (8.4 g in water (30 mL)) and the resulting mixture was extracted with DCM (50 mL) twice. The organic layer was washed with brine (30 mL) 2 times, dried over Na2SO4 and concentrated in vacuo to afford tert-butyl (2S)(methylamino)phenylpropanoate (710 mg, Compound AZ-1) as a light yellow oil.

Step 2: Preparation of (S)-tert-butyl 2-((chlorocarbonyl)(methyl)amino) phenylpropanoate (Intermediate AZ) N O AZ Intermediate AZ was prepared in analogy to intermediate AP by using utyl (2S) (methylamino)phenyl-propanoate (Compound AZ-1) instead of ethyl 2- (methylamino)acetate hydrochloride. The crude utyl (2S) [chlorocarbonyl(methyl)amino]phenyl-propanoate (360 mg, Intermediate AZ) was obtained as a light yellow oil and used for next step without further purification Intermediate BA N-[2-[acetyl(methyl)amino]ethyl]-N-methyl-carbamoyl chloride Step 1: Preparation of tert-butyl N-[2-[acetyl(methyl)amino]ethyl]-N-methyl-carbamate (Compound BA-1) To a on of tert-butyl methyl(2-(methylamino)ethyl)carbamate (1.13 g, 6 mmol) in pyridine (10 mL) was added acetic anhydride (3.06 g, 30 mmol) dropwise at 0oC. Then the solution was stirred at room temperature for 0.5 hr. The solvent was removed in vacuo and the residue was partitioned between EtOAc (50 mL) and saturated s NaHCO3 (25 mL). The organic layer was separated, washed with brine (20 mL), dried over Na2SO4 and concentrated in vacuo to afford tert-butyl N-[2-[acetyl(methyl)amino]ethyl]-N-methyl-carbamate (1.28 g, Compound BA-1) as a yellow oil.

Step 2: Preparation of N-methyl-N-(2-(methylamino)ethyl)acetamide hydrochloride (Compound BA-2) A mixture of utyl N-[2-[acetyl(methyl)amino]ethyl]-N-methyl-carbamate (1.1 g, Compound BA-1) in HCl/EtOAc (10 mL, 1N HCl in EtOAc) was stirred at room temperature for 2 hrs, then the mixture was filtered. The collected solid was washed with EtOAc (5 mL) three times and dried in vacuo to afford the crude yl-N-(2-(methylamino)ethyl)acetamide hydrochloride (460 mg, Compound BA-2) as a white solid.

Step 3: ation of N-[2-[acetyl(methyl)amino]ethyl]-N-methyl-carbamoyl chloride (Intermediate BA) Intermediate BA was ed in analogy to Intermediate AP by using N-methyl-N-(2- (methylamino)ethyl)acetamide hydrochloride (200 mg, Compound BA-2) instead of ethyl 2- (methylamino)acetate hydrochloride The crude N-[2-[acetyl(methyl)amino]ethyl]-N-methyl- carbamoyl chloride (300 mg, Intermediate BA) was obtained and used for next step without further purification.

Intermediate BB Methyl N-[2-[chlorocarbonyl(methyl)amino]ethyl]-N-methyl-carbamate Step 1: Preparation of methyl N-methyl-N-[2-(methylamino)ethyl]carbamate und BB-1) N O To a solution of N,N'-dimethylethane-1,2-diamine (10 g) in THF (40 mL) was added methyl chloroformate (1.92 g) dropwise at -70oC in 1 hr. The mixture was stirred at 25oC for 15 hrs and then filtered and washed with water and brine. The organic layer was dried and trated to afford a yellow residue, which was purified by column chromatography to afford methyl N-methyl-N-[2-(methylamino)ethyl]carbamate (2 g, Compound BB-1) as a colorless oil.

Step 2: ation of methyl N-[2-[chlorocarbonyl(methyl)amino]ethyl]-N-methyl- carbamate (Intermediate BB) Intermediate BB was prepared in analogy to Intermediate AP by using methyl N-methyl- N-[2-(methylamino)ethyl]carbamate (2.0 g, Compound BB-1) instead of ethyl 2- (methylamino)acetate hydrochloride. The crude methyl N-[2- ocarbonyl(methyl)amino]ethyl]-N-methyl-carbamate (2.2 g, Intermediate BB) was obtained and used for next step without further purification.

Intermediate BC tert-Butyl N-[2-[chlorocarbonyl(methyl)amino]ethyl]-N-methyl-carbamate Step 1: Preparation of tert-butyl N-methyl-N-[2-(methylamino)ethyl]carbamate (Compound BC-1) To a solution of N,N’-dimethylethane-1,2-diamine (40.4 g) in DCM (300 mL) was added a on of Boc2O (10 g, 10.6 mL, 45.8 mmol) in DCM (100 mL) dropwise at 0 oC over 1 hr.

The reaction mixture was stirred at room temperature for 18 hrs. The organic layer was washed with saturated aqueous NaHCO3 (50 mL), brine (50 mL), dried over Na2SO4 and trated in vacuo. The residue was purified by column chromatography to afford tert-butyl N-methyl-N-[2- (methylamino)ethyl]carbamate (6.8 g, Compound BC-1) as a yellow oil. 1H NMR (400MHz, CDCl3) δ ppm: 3.34 (br. s., 2H), 2.89 (s, 3H), 2.74 (t, J = 6.7 Hz, 2H), 2.46 (s, 3H), 1.47 (s, 9H).

Step 2: Preparation of tert-butyl N-[2-[chlorocarbonyl(methyl)amino]ethyl]-N-methylcarbamate (Intermediate BC) Intermediate BC was prepared in analogy to Intermediate AP by using tert-butyl N- -N-[2-(methylamino)ethyl]carbamate (1.15 g, Compound BC-1) instead of ethyl 2- (methylamino)acetate hydrochloride. The crude utyl N-[2- [chlorocarbonyl(methyl)amino]ethyl]-N-methyl-carbamate (1.3 g, Intermediate BC) was obtained and used for the next step without further purification.

Intermediate BD Ethyl N-[2-[chlorocarbonyl(methyl)amino]ethyl]-N-methyl-carbamate Step 1: Preparation of ethyl N-methyl-N-[2-(methylamino)ethyl]carbamate (Compound BD-1) N O To a solution of imethylethane-1,2-diamine (10 g) in DCM (40 mL) was added ethyl chloroformate (2.58 g) dropwise at -70oC in 1 hr. The reaction mixture was stirred at 25oC for 15 hrs and then filtered and washed with water and brine. The organic layer was dried and concentrated in vacuo. The yellow residue was purified by column chromatography to afford ethyl N-methyl-N-[2-(methylamino)ethyl]carbamate (2 g, Compound BD-1) as a colorless oil.

Step 2: Preparation of ethyl N-[2-[chlorocarbonyl(methyl)amino]ethyl]-N-methylcarbamate (Intermediate BD) Intermediate BD was prepared in analogy to Intermediate AA by using ethyl N-methyl- N-[2-(methylamino)ethyl]carbamate (Compound BD-1) instead of ethyl 2-(methylamino)acetate hydrochloride. The crude ethyl N-[2-[chlorocarbonyl(methyl)amino]ethyl]-N-methyl-carbamate (2.2 g, Intermediate BD) was obtained and used for the next step t further purification.

Intermediate BE 2-[Chlorocarbonyl(methyl)amino]ethyl N-butyl-N-methyl-carbamate Step 1: Preparation of utyl N-(2-hydroxyethyl)-N-methyl-carbamate (Compound BE- 1) O N To a solution of 2-(methylamino)ethanol (10 g, 133.14 mmol) in DCM (10 mL) was added Boc2O (34.87 g, 159.77 mmol) at 25 oC. The mixture was stirred at 25oC for 16 hrs and then concentrated. The residue was purified by column chromatography to afford utyl N-(2- hydroxyethyl)-N-methyl-carbamate (20 g, Compound BE-1) as a colorless oil.

Step 2: Preparation of 2-[tert-butoxycarbonyl(methyl)amino]ethyl N-butyl-N-methylcarbamate (Compound BE-2) To a solution of tert-butyl N-(2-hydroxyethyl)-N-methyl-carbamate (880 mg, Compound BE-1) and Et3N (1 g, 10.08 mmol) in DCM (10 mL) was added N-butyl-N-methyl-carbamoyl chloride (903 mg, 7.04 mmol) dropwise at -10oC in 1 hr. The reaction mixture was stirred at 25oC for 15 hrs and then ed and washed with water and brine. The c layer was dried and concentrated to afford 2-[tert-butoxycarbonyl(methyl)amino]ethyl N-butyl-N-methylcarbamate (2 g, Compound BE-2) as a ess oil.

Step 3: Preparation of 2-(methylamino)ethyl l-N-methyl-carbamate hydrochloride (Compound BE-3) BE-3 To a solution of 2-[tert-butoxycarbonyl(methyl)amino]ethyl N-butyl-N-methyl-carbamate (1 g, Compound BE-2) was added HCl/EA (40 mL, 1M). The reaction mixture was stirred at 0oC for 0.5 hr and warmed to 25 oC and d for another 15.5 hrs. The reaction mixture was concentrated to afford 2-(methylamino)ethyl-N-butyl-N-methyl-carbamate hydrochloride (400 mg, Compound BE-3) as a colorless oil.

Step 4: Preparation of 2-[chlorocarbonyl(methyl)amino]ethyl N-butyl-N-methyl-carbamate (Intermediate BE) Intermediate BE was prepared in analogy to Intermediate AP by using 2- (methylamino)ethyl N-butyl-N-methyl-carbamate hydrochloride (374 mg, Compound BE-3) instead of ethyl 2-(methylamino)acetate hloride. The crude 2- [chlorocarbonyl(methyl)amino]ethyl N-butyl-N-methyl-carbamate (330 mg, Intermediate BE) was obtained and used for next step without further purification.

Intermediate BF 2-[Chlorocarbonyl(methyl)amino]ethyl pyrrolidinecarboxylate Cl O O N O N Step 1: Preparation of tert-butyl N-(2-hydroxyethyl)-N-methyl-carbamate (Compound BF- To a solution of 2-(methylamino)ethanol (10 g, 133.14 mmol) in DCM (10 mL) was added Boc2O (34.87 g, 159.77 mmol) at 25 oC. The mixture was stirred at 25oC for 16 hrs. The reaction mixture was concentrated to give the residue, which was purified by column chromatography to afford tert-butyl ydroxyethyl)-N-methyl-carbamate (20 g, nd BF-1) as a colorless Step 2: Preparation of 2-[tert-butoxycarbonyl(methyl)amino]ethyl pyrrolidine carboxylate (Compound BF-2) O O O N O N To a on of tert-butyl N-(2-hydroxyethyl)-N-methyl-carbamate (300 mg, 1.71 mmol, nd BF-1) and Et3N (578 mg, 5.71 mmol) in DCM (5 mL) was added pyrrolidine carbonyl chloride (458 mg, 3.4 mmol) dropwise at 0oC for 0.5 hr and then stirred at 25oC for .5 hrs. After filtration, the filtrate was washed with water and brine. The organic layer was dried and concentrated to afford the 2-[tert-butoxycarbonyl(methyl)amino]ethyl pyrrolidine carboxylate (335 mg, Compound BF-2) as a colorless oil.

Step 3: Preparation of 2-(methylamino)ethyl pyrrolidinecarboxylate hydrochloride (Compound BF-3) N O N 2-[tert-butoxycarbonyl(methyl)amino]ethyl pyrrolidinecarboxylate (335 mg, nd BF-2) was added to HCl in EA (12.3 mL, 1M) and the mixture was stirred at 0oC for 0.5 hr and then at 25oC for another 15.5 hrs. The reaction mixture was concentrated to afford 2- (methylamino)ethyl pyrrolidinecarboxylate hydrochloride (300 mg, Compound BF-3) as a ess oil.

Step 4: Preparation of 2-[chlorocarbonyl(methyl)amino]ethyl pyrrolidinecarboxylate (Intermediate BF) Cl O O N O N Intermediate BF was prepared in analogy to Intermediate AP by using the 2- (methylamino)ethyl pyrrolidinecarboxylate hydrochloride (299 mg, Compound BF-3) instead of ethyl 2-(methylamino)acetate hydrochloride. The crude 2- ocarbonyl(methyl)amino]ethyl pyrrolidinecarboxylate (230 mg, Intermediate BF) was obtained and used for next step t further purification.

Intermediate BG 2-[Chlorocarbonyl(methyl)amino]ethyl N-methyl-N-propyl-carbamate Step 1: ation of tert-butyl N-(2-hydroxyethyl)-N-methyl-carbamate (Compound BG- O N BG-1 To a solution of 2-(methylamino)ethanol (10 g, 133.14 mmol) in DCM (10 mL) was added Boc2O (34.87 g, 159.77 mmol) at 25 oC. The reaction mixture was stirred at 25oC for 16 hrs, then concentrated to give the e, which was purified by column chromatography to afford tertbutyl N-(2-hydroxyethyl)-N-methyl-carbamate (20 g, Compound BG-1) as a colorless oil.

Step 2: Preparation of tert-butyl-N-methyl-N-[2-[methyl(propyl)carbamoyl]oxyethyl] carbamate (Compound BG-2) O O O N O N To a solution of tert-butyl N-(2-hydroxyethyl)-N-methyl-carbamate (265 mg, Compound BG-1) and Et3N (1 mL, 5.71 mmol) in DCM (5 mL) was added N-methyl-N-propyl-carbamoyl chloride (410 mg, 1.83 mmol) dropwise at 0oC for 0.5 hr. The reaction e was stirred at 25oC for 15.5 hrs and then filtered and the filtrate was washed with water and brine. The organic layer was dried and concentrated to afford tert-butyl N-methyl-N-[2- [methyl(propyl)carbamoyl]oxyethyl]carbamate (380 mg, nd BG-2) as a colorless oil.

Step 3: Preparation of hylamino)ethyl N-methyl-N-propyl-carbamate hydrochloride (Compound BG-3) utyl N-methyl-N-[2-[methyl(propyl)carbamoyl]oxyethyl]carbamate (380 mg, Compound BG-2) was added to HCl in EA (13.7 mL, 1M). The mixture was stirred at 0oC for 0.5 hr. Then the mixture was stirred at 25oC for another 15.5 hrs and concentrated to afford 2- (methylamino)ethyl yl-N-propyl-carbamate hydrochloride (300 mg, Compound BG-3) as a colorless oil.

Step 4: Preparation of 2-[chlorocarbonyl(methyl)amino]ethyl N-methyl-N-propyl- carbamate (Intermediate BG) Intermediate BG was prepared in analogy to Intermediate AP by using 2- lamino)ethyl N-methyl-N-propyl-carbamate hydrochloride (330 mg, Compound BG-3) instead of ethyl 2-(methylamino)acetate hydrochloride. The 2- [chlorocarbonyl(methyl)amino]ethyl-N-methyl-N-propyl-carbamate (300 mg, Intermediate BG) was obtained and used for next step without further purification.

Intermediate BH 2-[Chlorocarbonyl(methyl)amino]ethyl N,N-diethylcarbamate Step 1: Preparation of tert-butyl N-(2-hydroxyethyl)-N-methyl-carbamate (Compound BH- O N To a solution of 2-(methylamino)ethanol (10 g, 133.14 mmol) in DCM (10 mL) was added Boc2O (34.87 g, 159.77 mmol) at 25 oC. The mixture was stirred at 25oC for 16 hrs and then concentrated, the residue was purified by column chromatography to afford tert-butyl N-(2- hydroxyethyl)-N-methyl-carbamate (20 g, Compound BH-1) as a colorless oil.

Step 2: Preparation of 2-[tert-butoxycarbonyl(methyl)amino]ethyl-N,N-diethylcarbamate (Compound BH-2) BH-2 To a solution of tert-butyl N-(2-hydroxyethyl)-N-methyl-carbamate (200 mg, 1.14 mmol, Compound BH-1) and Et3N (578 mg, 5.71 mmol) in DCM (5 mL) was added N,N- diethylcarbamoyl chloride (248 mg, 1.83 mmol) dropwise at 0 oC for 0.5 hr and d at 25 oC for 15.5 hrs. After filtration, the te was washed with water and brine. The organic layer was dried and concentrated to afford the 2-[tert-butoxycarbonyl(methyl)amino]ethyl N,N- diethylcarbamate (313 mg, Compound BH-2) as a colorless oil.

Step 3: Preparation of hylamino)ethyl N,N-diethylcarbamate hydrochloride (Compound BH-3) t-butoxycarbonyl(methyl)amino]ethyl N,N-diethylcarbamate (436 mg, 1.77 mmol, Compound BH-2) was added to HCl in EA (17 mL, 1M). The mixture was stirred at 0oC for 0.5 hr. Then the mixture was stirred at 25oC for another 15.5 hrs and concentrated to afford 2- (methylamino)ethyl ethylcarbamate hydrochloride (230 mg, Compound BH-3) as a colorless oil.

Step 4: Preparation of 2-[chlorocarbonyl(methyl)amino]ethyl N,N-diethylcarbamate (Intermediate BH) Intermediate BH was prepared in analogy to Intermediate AP by using 2- (methylamino)ethyl N,N-diethylcarbamate hydrochloride (274 mg, Compound BH-3) instead of ethyl 2-(methylamino)acetate hydrochloride. The crude 2-[chlorocarbonyl(methyl)amino]ethyl N,N-diethylcarbamate (250 mg, Intermediate BH) was ed and used for next step without further cation.

Intermediate BI 2-[Chlorocarbonyl(methyl)amino]ethyl ethyl carbonate Step 1: Preparation of tert-butyl N-(2-hydroxyethyl)-N-methyl-carbamate (Compound BI-1) O O To a solution of 2-(methylamino)ethanol (1 g, 13.31 mmol) in DCM (10 mL) was added Boc2O (3.49 g, 15.98 mmol) at 25 oC. The reaction mixture was stirred at 25oC for 16 hrs, then trated to give the crude product, which was purified by column chromatography to afford tert-butyl N-(2-hydroxyethyl)-N-methyl-carbamate (1.6 g, Compound BI-1) as a colorless oil.

Step 2: Preparation of 2-[tert-butoxycarbonyl(methyl)amino]ethyl methyl ate (Compound BI-2) To a solution of tert-butyl ydroxyethyl)-N-methyl-carbamate (1 g, Compound BI-1), DMAP (0.1 g) and pyridine (1.15 g, 11.41 mmol) in EA (20 mL) was added methyl chloroformate (1.21 g, 11.15 mmol) dropwise at -10oC. The e was stirred at -10 oC for 1 hr.

The reaction mixture was filtered and the filtrate was washed with 5% citric acid and brine. The organic layer was dried and concentrated to afford 2-[tert-butoxycarbonyl(methyl)amino]ethyl methyl carbonate (1.22 g, Compound BI-2) as a colorless oil.

Step 3: Preparation of ethyl 2-(methylamino)ethyl carbonate hydrochloride (Compound BI-3) 2-[tert-butoxycarbonyl(methyl)amino]ethyl methyl carbonate (1.22 g, 4.94 mmol, Compound BI-2) was added to HCl in EA (10 mL, 40 mmol) and the mixture was stirred at 0 oC for 0.5 hr and at 25 oC for another 15.5 hrs. The reaction e was concentrated to afford ethyl 2-(methylamino)ethyl carbonate hydrochloride (1.06 g, Compound BI-3).

Step 4: ation of 2-[chlorocarbonyl(methyl)amino]ethyl ethyl carbonate (Intermediate BI) BI Intermediate BI was prepared in analogy to Intermediate AP by using ethyl 2- (methylamino)ethyl carbonate hydrochloride (150 mg, Intermediate BI-3) instead of ethyl 2- (methylamino)acetate hydrochloride. The crude 2-[chlorocarbonyl(methyl)amino]ethyl ethyl carbonate (145 mg, Intermediate BI) was obtained and used for next step without further cation.

PREPARATIVE EXAMPLES Example 1 6-Aminobenzyl-N-methyloxo-N-propyl(propylsulfonimidoyl)purinecarboxamide Method A: Step 1: Preparation of 4-aminobenzyloxo-1H-imidazolecarbonitrile (Compound 1a) To a solution of aminomalononitrile p-toluenesulfonate (25 g, 98.5 mmol, TCI, Catalog number: A1119-25G) in dry THF (100 mL) was added benzyl isocyanate (13.2 g, 98.5 mmol) and TEA (10.2 g, 79.0 mmol) at RT. After stirred at RT for 24 hrs, the reaction was concentrated in vacuo and the residue was partitioned between EtOAc (500 mL) and water (250 mL). The separated organic layer was washed with brine (50 mL) twice, and extracted with sodium hydroxide solution (50 mL, 1N) twice. The ed sodium hydroxide solution layer was neutralized with 10 wt.% sodium hydrogen sulfate solution and extracted with EtOAc. The ted organic layer was washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The residue was triturated in 2-isopropoxypropane and then the suspension was filtered to give 4-aminobenzyloxo-1H-imidazolecarbonitrile (15 g, Compound 1a) as a yellow solid. The product was used for the next step without r purification. MS obsd. (ESI+) [(M+H)+]: 215.

Step 2: Preparation of obenzylsulfanyl-7H-purinone (Compound 1b) HS N N 1b To a solution of 4-aminobenzyloxo-1H-imidazolecarbonitrile (15.0 g, 70.0 mmol, Compound 1a) in THF (700 mL) was added benzoylisothiocyanate (28.6 g, 175.1 mmol, TCI, Catalog number: A11596-100G) dropwise. After stirred at RT for 12 hrs, the reaction mixture was concentrated in vacuo. The residue was triturated in l ether (100 mL) and the ing precipitate was collected by filtration.

To a solution of the obtained precipitate in THF (700 mL) was added sodium hydroxide (70 mL, 2 N). The mixture was refluxed for 50 hrs, and then acidified to pH=3 with 10 wt.% aqueous sodium hydrogen sulfate solution. The resulting itate was collected by tion to give a crude 6-aminobenzylsulfanyl-7H-purinone (8.1 g, Compound 1b) as a yellow solid. The product was used for the next step without further purification. MS obsd. (ESI+) [(M+H)+]: 274.

Step 3: Preparation of 6-aminobenzyl(2-propylsulfanyl)-7H-purinone (Compound 1c To a solution of obenzylsulfanyl-7H-purinone (5.46 g, 20.0 mmol, Compound 1b) in DMF was added potassium carbonate (2.76 g, 20.0 mmol). And then 1- bromopropane (2.44 g, 20.0 mmol, TCI, Catalog number: B0638-500G) in DMF (5.0 mL) was slowly added to previous solution. After stirred at RT for 12 hrs, the reaction mixture was poured into water (200 mL), then acidified with 10 wt.% aqueous sodium hydrogen sulfate solution and ted with EtOAc (100 mL) twice. The organic layer was washed with brine, dried over Na2SO4 and concentrated in vacuo to give the crude product, which was purified by flash chromatography on silica gel to give 6-aminobenzyl(2-propylsulfanyl)-7H-purinone (4.8 g, Compound 1c) as a white solid. MS obsd. (ESI+) [(M+H)+]: 316.

Step 4: Preparation of 6-aminobenzylpropylsulfinyl-7H-purinone (Compound 1d) To a sion of compound 6-aminobenzyl(2-propylsulfanyl)-7H-purinone (2.7 g, 8.7 mmol, nd 1c) in OH (500 mL, V/V = 1:1) was added 3- chloroperbenzoic acid (2.15 g, 8.7 mmol, 70% purity, Aldrich, Catalog number: 273031-100G).

After on mixture was d for 2 hrs, the volume of reaction mixture was reduced in vacuo to about 50 mL. The resulting precipitate was collected by filtration, washed with methanol and dried to give 6-aminobenzylpropylsulfinyl-7H-purinone (1.0 g, Compound 1d) as a white solid. The product was used for the next step without further purification. MS obsd. (ESI+) [(M+H)+]: 332.

Step 5: Preparation of 6-aminobenzyl(propylsulfonimidoyl)-7H-purinone (Compound 1e) To a solution of 6-aminobenzylpropylsulfinyl-7H-purinone (1.52 g, 4.6 mmol, Compound 1d) in Eaton’s reagent (40 mL, phosphorus pentoxide, 7.5 wt. % in methanesulphonic acid, Aldrich, Catalog number: 380814-100ML) was added sodium azide (360 mg, 5.5 mmol) at 50 oC. After being stirred at this temperature for 30 minutes, the on mixture was cooled to RT and poured into sat. aqueous sodium bicarbonate solution. The reaction mixture was extracted with n-BuOH (100 mL) twice, and the organic phase was concentrated in vacuo. The residue was submitted for purification by prep-HPLC to give 6- aminobenzyl(propylsulfonimidoyl)-7H-purinone (1.2 g, Compound 1e) as a white solid. 1H NMR (400 MHz, DMSO-d 6) δ ppm: 10.65 (br. s., 1H), 7.26-7.37 (m, 5H), 6.98 (br. s., 2H), 4.97 (s, 2H), 4.02 (s, 1H), 3.33 (t, J = 7.53 Hz, 2H), 1.55-1.74 (m, 2H), 0.92 (t, J =7.53 Hz, 3H).

MS obsd. (ESI+) [(M+H)+]: 347.

Separation of compound 1e by chiral HPLC afforded Compound 1e-A (slower eluting, 500 mg) and Compound 1e-B r eluting, 490 mg) as white solid. (Separation condition: ol 5%-40% (0.05%DEA)/CO2 on ChiralPak AS-3 column.) nd 1e-A: 1H NMR (DMSO-d6, 400 MHz) δ ppm: 10.56 (s, 1H), 7.21 - 7.46 (m, 5H), 7.03 (s, 2H), 4.96 (s, 2H), 4.04 (s, 1H), 3.25 - 3.33 (m, 2H), 1.59 - 1.67 (m, 2H), 0.92 (t, J = 7.4 Hz, 3H).

Compound 1e-B: 1H NMR (DMSO-d6, 400 MHz) δ ppm: 10.57 (s, 1H), 7.23 - 7.39 (m, 5H), 6.97 (s, 2H), 4.96 (s, 2H), 4.05 (s, 1H), 3.31 - 3.30 (m, 2H), 1.49 - 1.74 (m, 2H), 0.91 (t, J = 7.4 Hz, 3H).

Step 6: ation of 6-aminobenzyl-N-methyloxo-N-propyl (propylsulfonimidoyl)purinecarboxamide (Example 1) To a solution of 6-aminobenzyl(propylsulfonimidoyl)-7H-purinone (300 mg, Compound 1e), pyridine (329 mg, 4.2 mmol) and DIPEA (538 mg, 4.2 mmol) in NMP (5 mL) was added N-methyl-N-propyl-carbamoyl chloride (564 mg, 4.2 mmol, Intermediate AA) at RT. The e was d at RT for 10 hrs. The reaction mixture was concentrated and the residue was purified by prep-HPLC to give 6-aminobenzyl-N-methyloxo-N-propyl (propylsulfonimidoyl)purinecarboxamide (108 mg, Example 1) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.45 - 7.24 (m, 5H), 6.89 (s, 2H), 5.01 (s, 2H), 4.17 (s, 1H), 3.44 - 3.34 (m, 2H), 3.36 - 3.34 (m, 2H), 3.10 - 3.00 (m, 3H), 1.74 - 1.52 (m, 4H), 1.01 - 0.72 (m, 6H).

MS obsd. (ESI+) [(M+H)+]: 446.

Separation of compound of Example 1 by chiral HPLC afforded Example 1-A (slower eluting, 50 mg) and Example 1-B (faster eluting, 40 mg) as white solid with isopropanol 5%- 40% (0.05%DEA)/CO2 on ChiralPak AD-3 .

Example 1-A: 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.44-7.24 (m, 5H), 6.89 (s, 2H), .01 (s, 2H), 4.17 (s, 1H), 3.44-3.37 (m, 2H), 3.37-3.35 (m, 2H), 3.10-3.00 (m, 3H), 1.74-1.52 (m, 4H), 1.00-0.72 (m, 6H). MS obsd. (ESI+) [(M+H)+]: 446.

Example 1-B: 1H NMR (400 MHz, DMSO-d6) δ ppm: .26 (m, 5H), 6.88 (s, 2H), .01 (s, 2H), 4.15 (s, 1H), 3.44-3.36 (m, 2H), 3.34 (s, 2H), 3.10-3.01 (m, 3H), 1.77-1.52 (m, 4H), 1.02-0.67 (m, 6H). MS obsd. (ESI+) [(M+H)+]: 446.

Method B: Alternative method to prepare 6-aminobenzyl(propylsulfonimidoyl)-7H- purinone (Compound 1e) Step 1: Preparation of N-benzylchloronitropropylsulfanyl-pyrimidinamine (Compound 1f) To a solution of 4,6-dichloronitropropylsulfanylpyrimidine (150.0 g, 559.5 mmol) and DIPEA (108.5 g, 839.2 mmol) in THF(1.5 L) was added phenylmethanamine (60.0 g, 559.5 mmol) in THF(200 mL) slowly at -78 °C. After addition, the mixture was warmed to 25 °C, and stirred at this temperature for 16 hrs. The resulting mixture was diluted with EA (1 L), washed with water (400 mL) three times and brine (500 mL). The separated c phase was dried over , filtered and concentrated in vacuo to give N-benzylchloronitro propylsulfanyl-pyrimidinamine (180.0 g, Compound 1f) as a yellow solid and used for next step t further purification. MS obsd. (ESI+) [(M+H)+]: 339.1.

Step 2: Preparation of N4-benzylchloropropylsulfanyl-pyrimidine-4,5-diamine (Compound 1g) To a solution of N-benzylchloronitropropylsulfanyl-pyrimidinamine (180 g, Compound 1f) and HOAc (319 g, 5.31 mol) in THF(3.0 L) was added Zn (174 g, 2.66 mol) slowly at 25°C. After the addition, the e was stirred at 25 °C for 16 hrs. The reaction was filtered and the filtrate was basified with saturated aq. NaHCO3 (800 mL), extracted with EA (400 mL) three times, dried over Na2SO4 and concentrated in vacuo. The e was purified by silica gel chromatography to give N4-benzylchloropropylsulfanyl-pyrimidine-4,5-diamine (125 g, Compound 1g) as a brown solid. MS obsd. (ESI+) [(M+H)+]: 309.1.

Step 3: Preparation of 9-benzylchloropropylsulfanyl-7H-purinone (Compound 1h) To a solution of N-benzylchloro(propylsulfanyl)pyrimidine-4,5-diamine (72.0 g, 233.1 mmol, Compound 1g) and CDI (75.2 g, 233.1 mmol) in THF(800mL) was d at 80°C for 16 hrs. The resulting mixture was diluted with EA (400 mL), washed with water (200 mL) twice and brine (200 mL). The separated organic layer was dried over Na2SO4, concentrated in vacuo. The e was washed with MTBE (200 mL) to give 9-benzylchloro propylsulfanyl-7H-purinone (58.0 g, Compound 1h) as a white solid and was used in next step without further purification. MS obsd. (ESI+) [(M+H)+]: 335.1.

Step 4: Preparation of 9-benzyl[(4-methoxyphenyl)methylamino]propylsulfanyl-7H- purinone (Compound 1i) A solution of 9-benzylchloropropylsulfanyl-7H-purinone (58.0 g, Compound 1h) and PMBNH2 (54.7 g, 398.42 mmol) in n-BuOH (600 mL) was stirred at 120 °C for 20 hrs. The reaction was concentrated and the residue was washed with MTBE (400 mL) to give 9-benzyl [(4-methoxyphenyl)methylamino]propylsulfanyl-7H-purinone (75 g, Compound 1i) as a white solid and was used in next step without further purification. MS obsd. (ESI+) [(M+H)+]: 436.2.

Step 5: Preparation of 6-aminobenzylpropylsulfanyl-7H-purinone (Compound 1c) 9-Benzyl[(4-methoxyphenyl)methylamino]propylsulfanyl-7H-purinone (87.0 g, Compound 1i) in TFA (200 mL) was stirred at 80 °C for 16 hrs. The resulting reaction mixture was concentrated, basified with saturated aq. NaHCO3 (600 mL). The resulting precipitate was collected by tion and washed with (PE/DCM = 2:1, 400mL) to give 6-aminobenzyl propylsulfanyl-7H-purinone (38.0 g, Compound 1c) as a white solid. MS obsd. (ESI+) [(M+H)+]: 316.1.

Step 6: Preparation of obenzylpropylsulfinyl-7H-purinone (Compound 1d) To a solution of m-CPBA(22.98 g, 113.2 mmol) in THF (50 mL) was added dropwise to a sion of 6-aminobenzylpropylsulfanyl-7H-purinone (35.0 g, compound 1c) in THF (200 mL) at 0 °C. After the addition, the on mixture was stirred at 25 °C for 0.5 hr.

The mixture was filtered and washed with MeCN (400 mL), MTBE (500 mL) to give 6-amino benzylpropylsulfinyl-7H-purinone (35.1 g, Compound 1d) as a white solid, which was used for the next step without further purification. MS obsd. (ESI+) [(M+H)+]: 332.1.

Step 7: Preparation of 6-aminobenzyl(propylsulfonimidoyl)-7H-purinone (Compound 1e) To a solution of 6-aminobenzylpropylsulfinyl-7H-purinone (34.0 g, Compound 1d) in Eaton's reagent (170.0 mL, 7.5 wt. % in methanesulphonic acid) was added NaN3 (15.34 g, 253.97 mmol) at 60 °C slowly. Then the e was stirred at 60 °C for 30 mins. The resulting reaction mixture was cooled to 25 °C, poured into ice cold O (500 mL, 1 mol/L), extracted with n-BuOH (100 mL) four times and concentrated in vacuo. The residue was purified by prep-HPLC to give 6-aminobenzyl(propylsulfonimidoyl)-7H-purinone (10 g, Compound 1e). 1H NMR (400 MHz, DMSO-d6) δ ppm: 10.65 (br. s., 1H), 7.26-7.37 (m, 5H), 6.98 (br. s., 2H), 4.97 (s, 2H), 4.02 (s, 1H), 3.33 (t, J = 7.53 Hz, 2H), .74 (m, 2H), 0.92 (t, J =7.53 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 347.

Example 2 6-Aminobenzyl-N-(2-methoxyethyl)-N-methyloxo(propylsulfonimidoyl)purine carboxamide The title compound was prepared in analogy to Example 1, Method A, Step 6 by using N- (2-methoxyethyl)-N-methyl-carbamoyl chloride (Intermediate AB) instead of N-methyl-N- propyl-carbamoyl chloride (Intermediate AA). 6-Aminobenzyl-N-(2-methoxyethyl)-N- methyloxo(propylsulfonimidoyl)purinecarboxamide (120 mg, e 2) was obtained as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.27-7.39 (m, 5H), 6.89 (br. s., 1H), 6.78 (br. s., 1H), 5.00 (s, 2H), 4.16 (br. d, J = 4 Hz, 1H), 3.62 (br. dd, J = 4, 12 Hz, 2H), 3.28- 3.42 (m, 6H), 3.12 (d, J = 12 Hz, 3H), 3.05 (s, 1H), 1.58-1.72 (m, 2H), 0.93 (t, J = 8 Hz, 3H).

MS obsd. (ESI+) [(M+H)+]: 462.

Separation of compound of Example 2 by chiral HPLC afforded Example 2-A (faster eluting, 33 mg) and Example 2-B r eluting, 46 mg) as white solid with methanol 5%-40% (0.05%DEA)/CO2 on ChiralPak OJ-3 column.

Example 2-A: 1H NMR (400 MHz, DMSO-d6) δ ppm: .39 (m, 5H), 6.89 (br. s., 1H), 6.78 (br. s., 1H), 5.00 (s, 2H), 4.16 (br. d, J = 4 Hz, 1H), 3.62 (br. dd, J = 4, 12 Hz, 2H), 3.28-3.42 (m, 6H), 3.12 (d, J = 12 Hz, 3H), 3.05 (s, 1H), .72 (m, 2H), 0.93 (t, J = 8Hz, 3H).

MS obsd. (ESI+) [(M+H)+]: 462.

Example 2-B: 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.27-7.39 (m, 5H), 6.89 (br. s., 1H), 6.78 (br. s., 1H), 5.00 (s, 2H), 4.16 (br. d, J = 4 Hz, 1H), 3.62 (br. dd, J = 4, 12 Hz, 2H), 3.28- 3.42 (m, 6H), 3.12 (d, J = 12 Hz, 3H), 3.05 (s, 1H), 1.58-1.72 (m, 2H), 0.93 (t, J = 8Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 462.

Example 3 6-Aminobenzyl-N-ethyloxo-N-propyl(propylsulfonimidoyl)purinecarboxamide The title compound was prepared in analogy to Example 1, Method A, Step 6 by using N- ethyl-N-propyl-carbamoyl chloride (Intermediate AC) instead of N-methyl-N-propyl-carbamoyl de (Intermediate AA). 6-Aminobenzyl-N-ethyloxo-N-propyl (propylsulfonimidoyl)purinecarboxamide (51 mg, Example 3) was obtained as a white solid. 1H NMR (400 MHz, DMSO-d 6) δ ppm: .39 (m, 5H), 6.85 (br. s., 2H), 4.99 (s, 2H), 4.20 (br. d, J = 8.0 Hz, 1H), 3.13-3.54 (m, 4H), 1.46-1.72 (m, 4H), 1.30-1.39 (m, 1H), 1.00-1.26 (m, 6H), 0.81-0.95 (m, 5H), 0.73 (t, J = 8 Hz, 1H). MS obsd. (ESI+) [(M+H)+]: 474.

Example 4 6-Aminobenzyl[4-(1-piperidyl)piperidinecarbonyl](propylsulfonimidoyl)purin- 8-one NH2 N O O S N N The title compound was prepared in analogy to Example 1, Method A , Step 6 by using (1,4'-bipiperidine)-1'-carbonyl chloride instead of N-methyl-N-propyl-carbamoyl de mediate AA). 6-Aminobenzyl[4-(1-piperidyl)piperidinecarbonyl] (propylsulfonimidoyl)purinone (55 mg, Example 4) was obtained as a white powder. 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.39 - 7.27 (m, 5H), 6.97 (br. s., 2H), 4.99 (s, 2H), 4.20 (br. s., 2H), 3.85 (d, J = 12.5 Hz, 1H), 3.43 - 3.15 (m, 3H), 2.96 (t, J = 12.3 Hz, 2H), 2.56 (m, 4H), 1.83 (m, 1H), 1.79 - 1.54 (m, 4H), 1.50 (br. s., 4H), 1.45 - 1.33 (m, 3H), 0.93 (t, J = 7.4 Hz, 3H).

MS obsd. (ESI+) [(M+H)+]: 541.2.

Example 5 6-Aminobenzyl-N-ethyl-N-(2-methoxyethyl)oxo(propylsulfonimidoyl)purine carboxamide NH2 N O O S N N The title compound was prepared in analogy to Example 1, Method A, Step 6 by using N- N-(2-methoxyethyl)carbamoyl chloride (Intermediate AD) instead of N-methyl-N-propylcarbamoyl chloride (Intermediate AA). 6-Aminobenzyl-N-ethyl-N-(2-methoxyethyl)oxo- pylsulfonimidoyl)purinecarboxamide (34 mg, Example 5) was obtained as a white powder. 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.39 - 7.28 (m, 5H), 6.89 (br. s., 1H), 6.74 (br. s., 1H), 4.99 (s, 2H), 4.17 (d, J = 8.1 Hz, 1H), 3.67 (br. s., 2H), 3.63 - 3.51 (m, 2H), 3.50 - 3.34 (m, 4H), 3.29 (s, 1H), 3.11 (s, 2H), 1.73 - 1.59 (m, 2H), 1.23 - 1.07 (m, 3H), 0.93 (t, J = 7.5 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 476.3.

Example 6 6-Aminobenzyl-N-butyl-N-ethyloxo(propylsulfonimidoyl)purinecarboxamide NH2 N O O S N N 6 The title compound was prepared in analogy to Example 1, Method A, Step 6 by using N- butyl-N-ethyl-carbamoyl chloride (Intermediate AE) instead of N-methyl-N-propyl-carbamoyl chloride (Intermediate AA). 6-Aminobenzyl-N-butyl-N-ethyloxo (propylsulfonimidoyl)purinecarboxamide (51 mg, Example 6) was ed as a white solid. 1H NMR (400 MHz, DMSO-d 6) δ ppm: 7.27-7.39 (m, 5H), 6.85 (br. s., 2H), 4.99 (s, 2H), 4.20 (br. d, J = 8.0 Hz, 1H), .54 (m, 4H), 1.46-1.72 (m, 4H), 1.30-1.39 (m, 1H), 1.00-1.26 (m, 6H), 0.81-0.95 (m, 5H), 0.73 (t, J = 8 Hz, 1H). MS obsd. (ESI+) [(M+H)+]: 474.

Example 7 6-Aminobenzyl-N-(2-methoxyethyl)oxo-N-propyl(propylsulfonimidoyl)purine carboxamide NH2 N O O S N N The title compound was prepared in analogy to Example 1, Method A, Step 6 by using N- ethyl-N-(2-methoxyethyl)carbamoyl chloride (Intermediate AF) instead of N-methyl-N-propylcarbamoyl chloride mediate AA). 6-aminobenzyl-N-(2-methoxyethyl)oxo-N-propyl- 2-(propylsulfonimidoyl)purinecarboxamide (35 mg, Example 7) was obtained as a white . 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.40 - 7.28 (m, 5H), 6.89 (br. s., 1H), 6.75 (br. s., 1H), 5.00 (d, J = 5.5 Hz, 2H), 4.24 - 4.16 (m, 1H), 3.77 (br. s., 1H), 3.67 (br. s., 1H), 3.62 - 3.53 (m, 1H), 3.42 - 3.27 (m, 5H), 3.23 - 3.02 (m, 3H), 1.66-1.38 (m, 4H), 0.96 - 0.70 (m, 6H).

MS obsd. (ESI+) [(M+H)+]: 490.5.

Example 8 6-Aminobenzyl-N,N-bis(2-methoxyethyl)oxo(propylsulfonimidoyl)purine carboxamide NH2 N N O O O S N N The title compound was prepared in analogy to Example 1, Method A, Step 6 by using bis(2-methoxyethyl)carbamic chloride (Intermediate AG) instead of N-methyl-N-propylcarbamoyl chloride mediate AA). 6-Aminobenzyl-N,N-bis(2-methoxyethyl)oxo (propylsulfonimidoyl)purinecarboxamide (35 mg, Example 8) was obtained as a white . 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.40 - 7.28 (m, 5H), 6.83 (br. s., 2H), 4.99 (s, 2H), 3.71 (br. s., 3H), 3.52 - 3.27 (m, 11H), 3.09 (s, 3H), 1.73 - 1.59 (m, 2H), 0.93 (t, J = 7.5 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 506.

Example 9 6-Amino(azetidinecarbonyl)benzyl(propylsulfonimidoyl)purinone The title compound was prepared in analogy to Example 1, Method A, Step 6 by using azetidinecarbonyl chloride (Intermediate AH) instead of yl-N-propyl-carbamoyl chloride (Intermediate AA). 6-Amino(azetidinecarbonyl)benzyl (propylsulfonimidoyl)purinone (120 mg, Example 9) was obtained as a white powder. 1HNMR (400 MHz, DMSO-d 6) δ ppm: 7.02 - 7.43 (m, 7H), 4.99 (s, 2H), 4.31 (t, J = 7.65 Hz, 2H), 4.08 - 4.23 (m, 3H), 3.34 - 3.41 (m, 2H), 2.28 (m, 2H), 1.56 - 1.73 (m, 2H), 0.93 (t, J = 7.40 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 430.

Example 10 6-Aminobenzyl-N-isopropyl-N-methyloxo(propylsulfonimidoyl)purine carboxamide NH2 N O O S N N 10 The title compound was prepared in y to e 1, Method A, Step 6 by using N- isopropyl-N-methyl-carbamoyl chloride (Intermediate AI) instead of N-methyl-N-propylcarbamoyl chloride (Intermediate AA). 6-Aminobenzyl-N-isopropyl-N-methyloxo (propylsulfonimidoyl)purinecarboxamide (97 mg, Example 10) was obtained as a white solid. 1H NMR (400 MHz, DMSO-d 6) δ ppm: 7.27-7.39 (m, 5H), 6.87 (br. s., 2H), 4.99 (s, 2H), 4.38- 4.45 (m, 1H), 4.09-4.21 (m, 1H), 3.29-3.43 (m, 2H), 2.89-2.95 (m, 3H), 1.58-1.73 (m, 2H), 1.21 (br d, J = 8 Hz, 6H), 0.93 (t, J = 8 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 446.

Example 11 6-Aminobenzyl(4-methylpiperazinecarbonyl)(propylsulfonimidoyl)purinone O N NH2 N O O S N N 11 The title compound was prepared in analogy to Example 1, Method A, Step 6 by using 4- methylpiperazinecarbonyl chloride instead of N-methyl-N-propyl-carbamoyl chloride mediate AA). 6-Aminobenzyl(4-methylpiperazinecarbonyl) (propylsulfonimidoyl)purinone (59.5 mg, e 11) was obtained as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.39 - 7.31 (m, 5H), 6.99 (s, 2H), 4.98 (s, 2H), 4.18 (s, 1H), 3.58 - 3.49 (m, 6H), 2.42 (m, 4H), 2.22 (s, 3H), 1.66 - 1.61 (m, 2H), 0.95 - 0.91 (t, J = 7.2 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 473.

Example 12 6-Aminobenzyl-N-(3-methoxypropyl)-N-methyloxo(propylsulfonimidoyl)purine carboxamide NH2 N O O S N N The title compound was ed in analogy to Example 1, Method A, Step 6 by using N- (3-methoxypropyl)-N-methyl-carbamoyl chloride instead of N-methyl-N-propyl-carbamoyl chloride (Intermediate AA). 6-Aminobenzyl-N-(3-methoxypropyl)-N-methyloxo (propylsulfonimidoyl)purinecarboxamide (92.2 mg, Example 12) was obtained as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.23 - 7.45 (m, 5H), 6.94 (s., 2H), 4.93-5.08 (m, 2H), 4.19 (s, 1H), 3.30 - 3.62 (m, 6H), 3.25 (s, 3H), 3.02 - 3.10 (m, 3H), 1.74 - 1.90 (m, 2H), 1.55 - 1.77 (m, 2H), 0.98 - 0.82 (m, 3H). MS obsd. (ESI+) [(M+H)+]: 476.3.

Example 13 6-Aminobenzyl-N-isobutyl-N-methyloxo(propylsulfonimidoyl)purine carboxamide The title compound was prepared in analogy to e 1, Method A, Step 6 by using N- isobutyl-N-methyl-carbamoyl de (Intermediate AL) instead of N-methyl-N-propyl- carbamoyl chloride (Intermediate AA). 6-Aminobenzyl-N-isobutyl-N-methyloxo (propylsulfonimidoyl)purinecarboxamide (64 mg, Example 13) was obtained as a white solid. 1H NMR (400 MHz, DMSO-d 6) δ ppm: 7.27-7.40 (m, 5H), 6.89 (br. s., 2H), 5.00 (s, 2H), 4.16 (br. s., 1H), 3.25-3.44 (m, 4H), 3.07 (s, 2H), 3.03 (s, 1H), 1.87-2.09 (m, 1H), 1.57-1.74 (m, 2H), 0.75-0.99 (m, 9H). MS obsd. (ESI+) [(M+H)+]: 460.

Example 14 Ethyl 2-[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl- amino]acetate O O NH2 N O O S N N The title compound was prepared in analogy to Example 1, Method A, Step 6 by using ethyl lorocarbonyl)(methyl)amino)acetate (Intermediate AP) instead of N-methyl-N- propyl-carbamoyl chloride (Intermediate AA). Ethyl 2-[[6-aminobenzyloxo lsulfonimidoyl)purinecarbonyl]-methyl-amino]acetate (38 mg, Example 14) was obtained as a light yellow powder. 1H NMR (400MHz, DMSO-d6) δ ppm: 7.41 - 7.27 (m, 5H), 6.82 (br. s., 1H), 5.04 - 4.95 (m, 2H), 4.35 (br. s., 1H), 4.28 (br. s., 1H), 4.23 - 4.16 (m, 2H), 4.08 (q, J = 7.2 Hz, 1H), 3.43 - 3.28 (m, 3H), 3.15 (s, 2H), 3.08 (s, 1H), 1.71 - 1.58 (m, 2H), 1.24 (t, J = 7.0 Hz, 2H), 1.12 (t, J = 7.0 Hz, 1H), 0.93 (t, J = 7.4 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 490.

Example 15 Ethyl aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino ]propanoate NH2 N O O S N N The title compound was prepared in analogy to Example 1, Method A, Step 6 by using ethyl 3-((chlorocarbonyl)(methyl)amino)propanoate instead of N-methyl-N-propyl-carbamoyl chloride mediate AA). Ethyl 3-[[6-aminobenzyloxo(propylsulfonimidoyl)purine- 7-carbonyl]-methyl-amino]propanoate (35 mg, Example 15) was obtained as a white powder. 1H NMR (400MHz, DMSO-d6) δ ppm: 7.43 - 7.26 (m, 5H), 6.93 (br. s., 2H), 4.99 (s, 2H), 4.16 (s, 1H), 4.08 (q, J = 7.1 Hz, 1H), 3.99 (d, J = 7.0 Hz, 1H), 3.67 (br. s., 2H), 3.40 - 3.29 (m, 2H), 3.08 (s, 2H), 2.99 (s, 1H), 2.71 (t, J = 6.4 Hz, 2H), 1.74 - 1.56 (m, 2H), 1.27 - 1.05 (m, 3H), 0.93 (t, J = 7.5 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 504.

Example 16 tert-Butyl 3-[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl- amino]propanoate The title compound was prepared in analogy to Example 1, Method A, Step 6 by using tert-butyl 3-[chlorocarbonyl(methyl)amino]propanoate mediate AR) d of N-methyl- N-propyl-carbamoyl chloride (Intermediate AA). tert-Butyl 3-[[6-aminobenzyloxo (propylsulfonimidoyl)purinecarbonyl]-methyl-amino]propanoate (60 mg, Example 16) was ed as a white powder. 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.41 - 7.27 (m, 5H), 6.93 (br. s., 2H), 4.99 (s, 2H), 4.15 (s, 1H), 3.64 (br. s., 2H), 3.51 - 3.33 (m, 2H), 3.08 (s, 2H), 2.98 (s, 1H), 2.62 (t, J = 6.9 Hz, 2H), 1.71 - 1.57 (m, 2H), 1.41 (s, 6H), 1.34 (s, 3H), 0.93 (t, J = 7.4 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 532.

Example 17 Ethyl (2S)[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino ]propanoate O O NH2 N O O S N N The title compound was ed in analogy to Example 1, Method A, Step 6 by using ethyl (2S)[chlorocarbonyl(methyl)amino]propanoate (Intermediate AS) instead of N-methyl- N-propyl-carbamoyl chloride (Intermediate AA). Ethyl (2S)[[6-aminobenzyloxo (propylsulfonimidoyl)purinecarbonyl]-methyl-amino]propanoate (34.1 mg, Example 17) was obtained as a yellow solid. 1H NMR (300 MHz, DMSO-d6) δ ppm: 7.22 - 7.49 (m, 5 H), 6.78 (br. s., 2H), 4.93 - 5.08 (m, 2H), 4.75 (br. s., 1H), 3.96 - 4.29 (m, 3H), 3.30 - 3.46 (m, 2H), 3.09 (s, 2H), 2.93 (br. s., 1H), 1.55 - 1.77 (m, 2H), 1.48 (d, J = 7.16 Hz, 3H), 1.09 - 1.29 (m, 3H), 0.94 (t, J = 7.44 Hz, 3H). MS obsd. (ESI+) +]: 504.2.

Example 18 tert-Butyl (2S)[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]- methyl-amino]methyl-pentanoate O O NH2 N O O S N N The title compound was prepared in analogy to Example 1, Method A, Step 6 by using tert-butyl (2S)[chlorocarbonyl(methyl)amino]methyl-pentanoate (Intermediate AT) instead of N-methyl-N-propyl-carbamoyl chloride (Intermediate AA). tert-Butyl -[[6- aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl-amino]methylpentanoate (22 mg, Example 18) was obtained as a white solid. 1H NMR (400MHz, DMSO-d6) δ ppm: 7.42 - 7.27 (m, 5H), 6.78 (br. s., 2H), 5.05 - 4.96 (m, 2H), 4.78 (br. s., 1H), 4.33 (br. s., 1H), 3.51 - 3.37 (m, 2H), 3.01 (s, 3H), 1.75 - 1.54 (m, 4H), 1.44 (s, 8H), 1.33 - 1.11 (m, 2H), 0.99 - 0.82 (m, 9H). MS obsd. (ESI+) [(M+H)+]: 574.3.

Example 19 Isopropyl (2S)[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]- methyl-amino]methyl-pentanoate The title compound was prepared in analogy to Example 1, Method A, Step 6 by using pyl (2S)[chlorocarbonyl(methyl)amino]methyl-pentanoate (Intermediate AU) instead of N-methyl-N-propyl-carbamoyl de (Intermediate AA). Isopropyl (2S)[[6- aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl-amino]methyl- pentanoate (43 mg, Example 19) was obtained as a white powder. 1H NMR (400MHz, DMSO- d6) δ ppm: 7.43 - 7.27 (m, 5H), 6.75 (br. s., 2H), 5.05 - 4.94 (m, 3H), 4.88 (br. s., 1H), 4.19 (br. s., 1H), 3.43 - 3.34 (m, 2H), 3.01 (s, 3H), 1.91 (br. s., 1H), 1.77 - 1.56 (m, 4H), 1.25 - 1.16 (m, 6H), 0.99 - 0.83 (m, 9H). MS obsd. (ESI+) [(M+H)+]: 560.3.

Example 20 Ethyl (2S)[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino thyl-butanoate The title compound was prepared in analogy to Example 1, Method A, Step 6 by using ethyl (2S)[chlorocarbonyl(methyl)amino]methyl-butanoate (Intermediate AV) instead of yl-N-propyl-carbamoyl chloride (Intermediate AA). Ethyl (2S)[[6-aminobenzyl oxo(propylsulfonimidoyl)purinecarbonyl]-methyl-amino]methyl-butanoate (51.5 mg, Example 20) was obtained as a white powder. 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.23 - 7.51 (m, 5H), 6.76 (br. s., 2H), 5.01 (br. s., 2H), 4.42 (br. s., 1H), 3.97 - 4.26 (m, 3H), 3.34 - 3.45 (m, 2H), 3.12 (br. s., 3H), 2.24 (br. s., 1H), 1.65 (br. s., 2H), 1.13 - 1.29 (m, 3H), 0.88 - 1.10 (m, 9H). MS obsd. (ESI+) [M+H+]: 532.2.

Example 21 Ethyl (2S)[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino ]methyl-pentanoate O O NH2 N O O S N N The title compound was prepared in analogy to Example 1, Method A, Step 6 by using ethyl (2S)[chlorocarbonyl(methyl)amino]methyl-pentanoate (Intermediate AW) instead of N-methyl-N-propyl-carbamoyl de (Intermediate AA). Ethyl (2S)[[6-aminobenzyl oxo(propylsulfonimidoyl)purinecarbonyl]-methyl-amino]methyl-pentanoate (17.3 mg, Example 21) was obtained as a white powder. 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.26 - 7.45 (m, 5H), 6.73 (br. s., 2H), 4.91 - 5.09 (m, 3H), 4.06 - 4.25 (m, 3H), 3.34 - 3.45 (m, 2H), 3.04 (br. s., 3H), 1.93 (br. s., 1H), 1.54 - 1.78 (m, 4H), 1.22 (t, J = 7.09 Hz, 3H), 0.77 - 1.01 (m, 9H).

MS obsd. (ESI+) [(M+H)+]: 546.3.

Example 22 Ethyl (2S)[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino ]phenyl-propanoate O O NH2 N O O S N N The title nd was prepared in analogy to Example 1, Method A, Step 6 by using ethyl -[chlorocarbonyl(methyl)amino]phenyl-propanoate (Intermediate AX) instead of N-methyl-N-propyl-carbamoyl chloride (Intermediate AA). Ethyl (2S)[[6-aminobenzyl oxo(propylsulfonimidoyl)purinecarbonyl]-methyl-amino]phenyl-propanoate (30 mg, e 22) was obtained as a white powder. 1H NMR (400MHz, DMSO-d6) δ ppm: 7.42 - 7.16 (m, 10H), 4.97 (s, 3H), 4.19 (q, J = 7.1 Hz, 2H), 3.35 - 3.15 (m, 6H), 3.10 - 2.90 (m, 3H), 1.71 - 1.46 (m, 2H), 1.28 - 1.18 (m, 4H), 0.97 - 0.85 (m, 3H). MS obsd. (ESI+) [(M+H)+]: 580.

Example 23 Isopropyl (2S)[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]- methyl-amino]phenyl-propanoate The title compound was prepared in analogy to e 1, Method A, Step 6 by using isopropyl (2S)[chlorocarbonyl(methyl)amino]phenyl-propanoate (Intermediate AY) instead of N-methyl-N-propyl-carbamoyl chloride (Intermediate AA). Isopropyl (2S)[[6- aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl-amino]phenylpropanoate (22 mg, e 23) was obtained as a white powder. 1H NMR (400MHz, DMSO- d6) δ ppm: 7.35 - 7.01 (m, 10H), 5.02-4.89 (m, 3H), 3.37-3.17 (m, 3H), 3.02 - 3.09 (m, 3H), 3.10 - 2.90 (m, 3H), 1.66 - 1.62 (m, 2H), 1.22 - 1.11 (m, 8H), 0.92 (t, J = 7.4 Hz, 3H). MS obsd.

(ESI+) [(M+H)+]: 594.

Example 24 tert-Butyl (2S)[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]- methyl-amino]phenyl-propanoate The title compound was prepared in analogy to Example 1, Method A, Step 6 by using tert-butyl (2S)[chlorocarbonyl(methyl)amino]phenyl-propanoate (Intermediate AZ) instead of yl-N-propyl-carbamoyl de (Intermediate AA). tert-Butyl (2S)[[6- aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl-amino]phenylpropanoate (34 mg, Example 24) was obtained as a white powder. 1H NMR (400MHz, DMSO- d6) δ ppm: 7.42 - 7.16 (m, 10H), 5.03 - 4.90 (m, 3H), 3.68 - 3.24 (m, 5H), 3.24 - 3.09 (m, 2H), 3.01 (s, 3H), 1.68 - 1.57 (m, 2H), 1.43 (s, 9H), 0.99 - 0.85 (m, 3H). MS obsd. (ESI+) [(M+H)+]: 608.3.

Example 25 Acetyl(methyl)amino]ethyl]aminobenzyl-N-methyloxo (propylsulfonimidoyl)purinecarboxamide The title compound was prepared in analogy to Example 1, Method A, Step 6 by using N- [2-[acetyl(methyl)amino]ethyl]-N-methyl-carbamoyl chloride (Intermediate BA) instead of N- methyl-N-propyl-carbamoyl chloride (Intermediate AA). N-[2-[Acetyl(methyl)amino]ethyl] aminobenzyl-N-methyloxo(propylsulfonimidoyl)purinecarboxamide (26.1 mg, Example 25) was obtained as a white powder.1H NMR (400MHz, 6) δ ppm: 7.43 - 7.27 (m, 5H), 7.02 (br, 2H), 5.04 - 4.97 (m, 2H), 4.19 - 4.13 (m, 1H), 3.57 (d, J = 5.5 Hz, 2H), 3.49 - 3.34 (m, 2H), 3.14 (s, 1H), 3.12 - 3.02 (m, 4H), 2.86 (d, J = 7.5 Hz, 2H), 2.69 - 2.64 (m, 1H), 2.05 (s, 1H), 1.99 (s, 1H), 1.91 - 1.83 (m, 1H), 1.70 - 1.59 (m, 2H), 0.97 - 0.90 (m, 3H). MS obsd. (ESI+) +]: 503.2.

Example 26 Methyl N-[2-[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino ]ethyl]-N-methyl-carbamate 26 The title compound was prepared in analogy to Example 1, Method A, Step 6 by using methyl N-[2-[chlorocarbonyl(methyl)amino]ethyl]-N-methyl-carbamate (Intermediate BB) instead of N-methyl-N-propyl-carbamoyl chloride (Intermediate AA). Methyl N-[2-[[6-amino- 9-benzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl-amino]ethyl]-N-methyl- carbamate (65 mg, Example 26) was obtained as a yellow solid. 1H NMR (400 MHz, CDCl3) δ ppm: 7.29 - 7.49 (m, 5H), 5.63 - 5.92 (m, 2H), 5.03 - 5.17 (m, 2H), 3.43 - 3.69 (m, 8H), 3.13 - 3.27 (m, 3H), 2.96 - 3.05 (m, 2H), 2.72 (br. s., 1H), 1.05 (t, J = 7.40 Hz, 3H), 1.87 (dd, J = 14.12, 6.96 Hz, 2H). MS obsd. (ESI+) [(M+H)+]: 519.2.

Example 27 tert-Butyl [6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]- methyl-amino]ethyl]-N-methyl-carbamate The title compound was prepared in analogy to Example 1, Method A, Step 6 by using tert-butyl N-[2-[chlorocarbonyl(methyl)amino]ethyl]-N-methyl-carbamate (Intermediate BC) instead of N-methyl-N-propyl-carbamoyl chloride (Intermediate AA). tert-Butyl N-[2-[[6- 9-benzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl-amino]ethyl]-N- methyl-carbamate (32 mg, Example 27) was obtained as a white powder. 1H NMR (400MHz, DMSO-d6) δ ppm: 7.43 - 7.26 (m, 5H), 6.89 (br. s., 2H), 4.99 (d, J = 5.0 Hz, 2H), 4.16 (s, 1H), 3.55 (br. s., 2H), 3.48 - 3.34 (m, 2H), 3.10 (s, 2H), 3.07 (s, 1H), 2.86 (d, J = 12.8 Hz, 2H), 2.74 (d, J = 9.5 Hz, 1H), 2.70 - 2.60 (m, 1H), 1.72 - 1.54 (m, 2H), 1.39 (s, 6H), 1.23 (s, 2H), 1.13 (s, 2H), 0.93 (t, J = 7.4 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 562.

Example 28 Ethyl N-[2-[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino ]ethyl]-N-methyl-carbamate The title compound was prepared in y to Example 1, Method A, Step 6 by using ethyl N-[2-[chlorocarbonyl(methyl)amino]ethyl]-N-methyl-carbamate (Intermediate BD) instead of N-methyl-N-propyl-carbamoyl chloride (Intermediate AA). Ethyl N-[2-[[6-amino benzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl-amino]ethyl]-N-methylcarbamate (87 mg, Example 28) was obtained as a yellow solid.1H NMR (400 MHz, CDCl3) δ ppm: 7.29 - 7.53 (m, 5H), 5.65 - 5.90 (m, 2H), 5.02 - 5.14 (m, 2H), 3.38 - 4.21 (m, 9H), 3.14 - 3.26 (m, 3H), 3.00 (br. s., 2H), 2.73 (s, 1H), 1.76 - 1.99 (m, 2H), 1.22 - 1.31 (m, 3H), 1.05 (s, 3H). MS obsd. (ESI+) [(M+H)+]: 533.2.

Example 29 2-[[6-Aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl- amino]ethyl N-butyl-N-methyl-carbamate NH2 N O O S N N The title compound was prepared in analogy to e 1, Method A, Step 6 by using 2- ocarbonyl(methyl)amino]ethyl N-butyl-N-methyl-carbamate (Intermediate BE) instead of N-methyl-N-propyl-carbamoyl chloride (Intermediate AA). 2-[[6-Aminobenzyloxo (propylsulfonimidoyl)purinecarbonyl]-methyl-amino]ethyl N-butyl-N-methyl-carbamate (19 mg, Compound 29) was obtained as yellow solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.25 - 7.48 (m, 5H), 6.96 (br. s., 2H), 4.99 (s, 2H), 4.06 - 4.36 (m, 3H), 3.59 - 3.83 (m, 1H), 3.33 - 3.49 (m, 3H), 3.07 - 3.21 (m, 4H), 2.79 (s, 2H), 1.65 (br. s., 2H), 1.05 - 1.47 (m, 6H), 0.93 (t, J = 7.40 Hz, 3H), 0.70 - 0.87 (m, 3H). MS obsd. (ESI+) [(M+H)+]: 561.2.

Example 30 Aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino ]ethyl pyrrolidinecarboxylate NH2 N O O S N N The title compound was prepared in analogy to Example 1, Method A, Step 6 by using 2- ocarbonyl(methyl)amino]ethyl pyrrolidinecarboxylate (Intermediate BF) instead of N- methyl-N-propyl-carbamoyl chloride (Intermediate AA). 2-[[6-Aminobenzyloxo (propylsulfonimidoyl)purinecarbonyl]-methyl-amino]ethyl pyrrolidinecarboxylate (10.0 mg, Example 30) was obtained as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.26 - 7.41 (m, 5H), 6.96 (br.s., 2H), 4.99 (s, 2H), 4.01 - 4.35 (m, 4H), 3.29 - 3.47 (m, 3H), 3.23 (br. s., 3H), 3.03 - 3.17 (m, 4H), 1.52 - 1.84 (m, 6H), 0.90 – 0.96 (m, 3H). MS obsd. (ESI+) [(M+H)+]: 545.2.

Example 31 2-[[6-Aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino ]ethyl yl-N-propyl-carbamate The title compound was prepared in analogy to e 1, Method A, Step 6 by using 2- [chlorocarbonyl(methyl)amino]ethyl N-methyl-N-propyl-carbamate (Intermediate BG) instead of N-methyl-N-propyl-carbamoyl chloride (Intermediate AA). 2-[[6-Aminobenzyloxo (propylsulfonimidoyl)purinecarbonyl]-methyl-amino]ethyl N-methyl-N-propyl-carbamate (3.7 mg, Example 31) was obtained as a yellow solid. 1H NMR (400 MHz, CD3OD) δ ppm: 7.22 - 7.48 (m, 5H), 5.09 - 5.22 (m, 4H), 4.55 (s, 2H), 3.38 - 3.57 (m, 4H), 3.13 (s, 3H), 1.61 - 1.85 (m, 4H), 1.22 - 1.41 (m, 3H), 0.88 - 1.13 (m, 6H). MS obsd. (ESI+) [(M+H)+]: 547.2.

Example 32 Aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino ]ethyl N,N-diethylcarbamate NH2 N O O S N N The title compound was ed in analogy to Example 1, Method A, Step 6 by using 2- [chlorocarbonyl(methyl)amino]ethyl N,N-diethylcarbamate mediate BH) instead of N- methyl-N-propyl-carbamoyl chloride (Intermediate AA). 2-[[6-Aminobenzyloxo (propylsulfonimidoyl)purinecarbonyl]-methyl-amino]ethyl N,N-diethylcarbamate (21.7 mg, Example 32) was obtained as yellow solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.25 - 7.41 (m, 5H), 6.96 (br. s., 2H), 4.99 (s, 2H), 4.08 - 4.36 (m, 3H), 3.70 (br, 1H), 3.33 - 3.46 (m, 3H), 3.01 - 3.24 (m, 7H), 1.55 - 1.74 (m, 2H), 0.86 - 1.05 (m, 9H). MS obsd. (ESI+) [(M+H)+]: 547.2.

Example 33 2-[[6-Aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl- amino]ethyl ethyl carbonate The title compound was prepared in analogy to Example 1, Method A, Step 6 by using 2- [chlorocarbonyl(methyl)amino]ethyl ethyl carbonate (Intermediate BI) instead of N-methyl-N- propyl-carbamoyl de (Intermediate AA). 2-[[6-Aminobenzyloxo (propylsulfonimidoyl)purinecarbonyl]-methyl-amino]ethyl ethyl carbonate (46 mg, Example 33) was ed as yellow solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 0.82 - 0.99 (m, 3H), 1.02 - 1.28 (m, 3H), 1.56 - 1.76 (m, 2H), 3.05 - 3.18 (m, 3H), 3.35 - 3.48 (m, 3H), 3.73 (t, J = .08 Hz, 2H), 4.08 - 4.27 (m, 3H), 4.37 (br. s., 1H), 5.00 (s, 2H), 6.76 - 7.11 (m, 2H), 7.22 - 7.45 (m, 5H). MS obsd. (ESI+) [(M+H)+]: 520.

Example 34-A and Example 34-B 6-Amino-N-butyl[(4-chlorophenyl)methyl]-N-methyloxo[S(S)- propylsulfonimidoyl]purinecarboxamide and 6-amino-N-butyl[(4- chlorophenyl)methyl]-N-methyloxo[S(S)-propylsulfonimidoyl]purinecarboxamide Step 1: Preparation of 4-amino[(4-chlorophenyl)methyl]oxo-1H-imidazole carbonitrile (Compound 34a) N H H2N N Compound 34a was prepared in analogy to Example 1, Method A, Step 1 by using 4- chlorobenzyl isocyanate instead of benzyl isocyanate. 4-Amino[(4-chlorophenyl)methyl] -imidazolecarbonitrile (8.0 g, Compound 34a) was obtained as a yellow solid. MS obsd. (ESI+) [(M+H)+]: 249.

Step 2: Preparation of 6-amino[(4-chlorophenyl)methyl]sulfanyl-7H-purinone (Compound 34b) N N HS N N Compound 34b was prepared in analogy to e 1, Method A, Step 2 by using 4- Amino[(4-chlorophenyl)methyl]oxo-1H-imidazolecarbonitrile und 34a) instead of 4-aminophenylmethyloxo-1H-imidazolecarbonitrile (Compound 1a). 6-Amino [(4-chlorophenyl)methyl]sulfanyl-7H-purinone (6.4 g, Compound 34b) was obtained as a yellow solid and was used for the next step without further purification. MS obsd. (ESI+) [(M+H)+]: 308.

Step 3: Preparation of 6-amino[(4-chlorophenyl)methyl]propylsulfanyl-7H-purin one (Compound 34c) Compound 34c was prepared in analogy to Example 1, Method A, Step 3 by using 6- amino[(4-chlorophenyl)methyl]sulfanyl-7H-purinone (Compound 34b) instead of 6- aminophenylmethylsulfanyl-7H-purinone (Compound 1b). 6-Amino[(4- chlorophenyl)methyl]propylsulfanyl-7H-purinone (800 mg, Compound 34c) was ed as a white solid. MS obsd. (ESI+) [(M+H)+]: 350.

Step 4: Preparation of 6-amino[(4-chlorophenyl)methyl]propylsulfinyl-7H-purin one und 34d) Compound 34d was prepared in analogy to Example 1, Method A, Step 4 by using 6- amino[(4-chlorophenyl)methyl]propylsulfanyl-7H-purinone (Compound 34c) instead of 6-aminobenzylpropylsulfanyl-7H-purinone (Compound 1c). 6-Amino[(4- chlorophenyl)methyl]propylsulfinyl-7H-purinone (150 mg, Compound 34d) was obtained as a white solid. MS obsd. (ESI+) [(M+H)+]: 366.

Step 5: ation of 6-amino[(4-chlorophenyl)methyl](propylsulfonimidoyl)-7H- purinone (compound 34e), 6-amino[(4-chlorophenyl)methyl][S(S)- propylsulfonimidoyl)-7H-purinone and 6-amino[(4-chlorophenyl)methyl][S(S)- propylsulfonimidoyl)-7H-purinone (Compound 34e-A and Compound 34e-B) 34e-A and 34e-B Compound 34e was prepared in analogy to Example 1, Method A, Step 5 by using 6- amino[(4-chlorophenyl)methyl]propylsulfinyl-7H-purinone (Compound 34d) instead of 6-aminobenzyl(2-propylsulfinyl)-7H-purinone (Compound 1d). 6-Amino[(4- chlorophenyl)methyl](propylsulfonimidoyl)-7H-purinone (250 mg, compound 34e) was ed as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 10.60 (br. s, 1H), 7.32-7.42 (m, 4H), 6.98 (br. s, 2H), 4.96 (s, 2H), 4.03 (s, 1H), 3.25-3.41 (m, 2H), 1.56-1.68 (m, 2H), 0.91 (t, J = 8 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 381.

Separation of compound of Compound 34e by chiral HPLC afforded Compound 34e-A (faster eluting, 110 mg) and Compound 34e-B (slower eluting, 100 mg) as white solid with ol 5%-40% (0.05%DEA)/CO2 on ChiralPak OJ-3 column.

Compound 34e-A: 1H NMR (400 MHz, DMSO-d6) δ ppm: 10.63 (br. s, 1H), 7.33-7.42 (m, 4H), 6.99 (br. s, 2H), 4.96 (s, 2H), 4.05 (br. s, 1H), 3.26-3.39 (m, 2H), .69 (m, 2H), 0.91 (t, J = 7.4 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 381.

Compound 34e-B: 1H NMR (400 MHz, DMSO-d6) δ ppm: 10.63 (br. s, 1H), 7.33-7.42 (m, 4H), 6.99 (br. s, 2H), 4.96 (s, 2H), 4.05 (br. s, 1H), .40 (m, 2H), 1.54-1.69 (m, 2H), 0.91 (t, J = 7.5 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 381.

Step 6: 6-Amino-N-butyl[(4-chlorophenyl)methyl]-N-methyloxo[S(S)- propylsulfonimidoyl]purinecarboxamide and 6-amino-N-butyl[(4- chlorophenyl)methyl]-N-methyloxo[S(S)-propylsulfonimidoyl]purinecarboxamide (Example 34-A and Example 34-B) Example 34-A was prepared in analogy to Example 1, Method A, Step 6 by using Compound 34e-A and N-butyl-N-methyl-carbamoyl chloride instead of 6-aminobenzyl (propylsulfonimidoyl)-7H-purinone (Compound 1e) and N-methyl-N-propyl-carbamoyl de (Intermediate AA).

Example 34-A (160 mg): 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.37-7.45 (m, 4H), 6.91 (br. s., 2H), 4.99 (s, 2H), 4.17 (s, 1H), 3.28-3.40 (m, 4H), 3.05 (s, 2H), 3.02 (s, 1H), 1.49-1.70 (m, 4H), 1.15-1.37 (m, 2H), 0.89-0.94 (m, 5H), 0.76 (t, J = 8 Hz, 1H). MS obsd. (ESI+) +]: 494. e 34-B (167 mg) was prepared in analogy to e 34-A by using Compound 34e-B instead of Compound 34e-A.

Example 34-B: 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.36-7.45 (m, 4H), 6.91 (br. s., 2H), 4.99 (s, 2H), 4.17 (s, 1H), 3.28-3.41 (m, 4H), 3.05 (s, 2H), 3.02 (s, 1H), 1.50-1.71 (m, 4H), 1.15- 1.37 (m, 2H), 0.89-0.94 (m, 5H), 0.76 (t, J = 7.4 Hz, 1H). MS obsd. (ESI+) [(M+H)+]: 494.

Example 35 6-Amino[(4-chlorophenyl)methyl]-N-ethyl-N-methyloxo (propylsulfonimidoyl)purinecarboxamide NH2O N O O S N N The title compound was ed in analogy to Example 1, Method A, Step 6 by using 6- amino[(4-chlorophenyl)methyl](propylsulfonimidoyl)-7H-purinone (Compound 34e) and N-ethyl-N-methyl-carbamoyl chloride instead of 6-aminobenzyl(propylsulfonimidoyl)- 7H-purinone (Compound 1e) and N-methyl-N-propyl-carbamoyl chloride (Intermediate AA). 6-Amino[(4-chlorophenyl)methyl]-N-ethyl-N-methyloxo (propylsulfonimidoyl)purinecarboxamide (60 mg, Example 35) was obtained as a white solid. 1H NMR (400 MHz, DMSO-d 6) δ ppm: 7.40 (s, 4H), 6.91 (br s, 2H), 4.99 (s, 2H), 4.16 (s, 1H), 3.34-3.44 (m, 4H), 3.05 (s, 2H), 3.01 (s, 1H), .67 (m, 2H), 1.18 (t, J = 8.0 Hz, 3H), 0.92 (t, J = 8.0 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 466.

Example 36-A and e 36-B 6-Amino-N-methyloxo-N-propyl-2[S(S)-propylsulfonimidoyl](p-tolylmethyl)purine carboxamide and 6-amino-N-methyloxo-N-propyl-2[S(R)-propylsulfonimidoyl](ptolylmethyl )purinecarboxamide NH2O N NH2O N N N N N HN O O O S N N S N N O HN Step 1: Preparation of 6-chloronitropropylsulfanyl-N-(p-tolylmethyl)pyrimidin amine (Compound 36a) Compound 36a was prepared in y to Example 1, Method B, Step 1 by using ptolylmethylamine instead of methanamine. 6-Chloronitropropylsulfanyl-N-(p- tolylmethyl)pyrimidinamine (3.9 g, Compound 36a) was obtained as a white solid. MS obsd.

(ESI+) [(M+H)+]: 353.

Step 2: Preparation of 6-chloropropylsulfanyl-N4-(p-tolylmethyl)pyrimidine-4,5-diamine (Compound 36b) S N NH Compound 36b was prepared in analogy to Example 1, Method B, Step 2 by using 6- chloronitropropylsulfanyl-N-(p-tolylmethyl)pyrimidinamine (Compound 36a) instead of N-benzylchloronitropropylsulfanyl-pyrimidinamine (Compound 1f). 6-Chloro propylsulfanyl-N4-(p-tolylmethyl)pyrimidine-4,5-diamine (2.2 g, Compound 36b) was obtained as a white solid. MS obsd. (ESI+) [(M+H)+]: 323.

Step 3: Preparation of 6-chloropropylsulfanyl(p-tolylmethyl)-7H-purinone (Compound 36c) Compound 36c was prepared in analogy to Example 1, Method B, Step 3 by using 6- chloropropylsulfanyl-N4-(p-tolylmethyl)pyrimidine-4,5-diamine (Compound 36b) instead of N-benzylchloro(propylsulfanyl)pyrimidine-4,5-diamine (Compound 1g). 6-Chloro propylsulfanyl(p-tolylmethyl)-7H-purinone (2.2 g, Compound 36c) was obtained as a white solid. MS obsd. (ESI+) +]: 349.

Step 4: ation of 6-[(4-methoxyphenyl)methylamino]propylsulfanyl(p- tolylmethyl)-7H-purinone (Compound 36d) NHPMB S N N Compound 36d was prepared in analogy to Example 1, Method B, Step 4, by using 6- propylsulfanyl(p-tolylmethyl)-7H-purinone (Compound 36c) instead of 9- benzylchloropropylsulfanyl-7H-purinone (Compound 1h). 6-[(4- methoxyphenyl)methylamino]propylsulfanyl(p-tolylmethyl)-7H-purinone (2.0 g, Compound 36d) was obtained as a white solid. MS obsd. (ESI+) [(M+H)+]: 450.

Step 5: Preparation of 6-aminopropylsulfanyl(p-tolylmethyl)-7H-purinone (Compound 36e) Compound 36e was ed in analogy to Example 1, Method B, Step 5 by using 6-[(4- methoxyphenyl)methylamino]propylsulfanyl(p-tolylmethyl)-7H-purinone (Compound 36d) instead of 6-aminobenzylpropylsulfanyl-7H-purinone (Compound 1i). 6-amino propylsulfanyl(p-tolylmethyl)-7H-purinone (1.0 g, Compound 36e) was obtained as a white solid. MS obsd. (ESI+) [(M+H)+]: 330.

Step 6: ation of 6-aminopropylsulfinyl(p-tolylmethyl)-7H-purinone (Compound 36f) NH2 H N N S N N Compound 36f was prepared in analogy to Example 1, Method B, Step 6 by using 6- aminopropylsulfanyl(p-tolylmethyl)-7H-purinone (Compound 36e) instead of 6-amino- 9-benzyl(2-propylsulfanyl)-7H-purinone und 1c). 6-aminopropylsulfinyl(p- tolylmethyl)-7H-purinone (220 mg, Compound 36f) was obtained as a white solid MS obsd.

(ESI+) [(M+H)+]: 345.

Step 7: Preparation of 6-amino(propylsulfonimidoyl)(p-tolylmethyl)-7H-purinone (Compound 36g) Compound 36g was ed in analogy to Example 1, Method B, Step 7 by using 6- aminopropylsulfinyl(p-tolylmethyl)-7H-purinone (Compound 36f) instead of 6-amino- 9-benzylpropylsulfinyl-7H-purinone (Compound 1d). 6-Amino(propylsulfonimidoyl)- 9-(p-tolylmethyl)-7H-purinone (127 mg, Compound 36g) was obtained as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 10.67 (br. s., 1H), 7.23 (d, J = 8.0 Hz, 2H), 7.13 (d, J = 8.0 Hz, 2H), 6.98 (br. s., 2H), 4.91 (s, 2H), 4.05 (s, 1H), 3.34-3.27 (m, 2H), 2.26 (s, 3H), 1.67-1.62 (m, 2H), 0.92 (t, J = 8.0 Hz, 3H). MS obsd. (ESI+) +]: 361.

Separation of compound 36g by chiral HPLC afforded compound 36g-A (faster g, 50 mg) and compound 36g-B (slower eluting, 49 mg) as white solid with 30% isopropanol (0.05%DEA)/CO2 on ChiralPak AD-3 column.

Compound 36g-A: 1H NMR: (400 MHz, DMSO-d6) δ ppm: 10.51 (s, 1 H), 7.22 (d, J = 8.0 Hz, 2H), 7.12 (d, J = 8.0 Hz, 2H), 7.00 (s, 2 H), 4.91 (s, 2H), 4.03 (s, 1H), 3.35 - 3.31 (m, 2H), 2.26 (s, 3H), 1.70 - 1.58 (m, 2H), 0.93 (t, J = 7.40 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 361.

Compound 36g-B: 1H NMR: (400 MHz, DMSO-d6) δ ppm: 10.54 (s, 1H), 7.23 (d, J = 8.0 Hz, 2H), 7.13 (d, J = 8.0 Hz, 2H), 6.97 (s, 2H), 4.91 (s, 2H), 4.04 (s, 1H), 3.34 - 3.30 (m, 2H), 2.26 (s, 3H), 1.72 - 1.57 (m, 2H), 0.93 (t, J = 7.40 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 361.

Step 8: Preparation of o-N-methyloxo-N-propyl-2[S(S)-propylsulfonimidoyl] (p-tolylmethyl)purinecarboxamide and 6-amino-N-methyloxo-N-propyl-2[S(R)- propylsulfonimidoyl](p-tolylmethyl)purinecarboxamide (Example 36-A and Example 36-B) NH2O N HN O S N N Example 36-A was prepared in analogy to Example 1, Method A, Step 6 by using Compound 36g-A instead of obenzyl(propylsulfonimidoyl)-7H-purinone (Compound 1e). Example 36-A (108 mg) was obtained as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.27 (d, J = 8 Hz, 2H), 7.14 (d, J = 8 Hz, 2H), 6.87 (br. s., 2H), 4.95 (s, 2H), 4.15 (s, 1H), 3.33-3.57 (m, 4H), 3.05 (s, 2H), 3.02 (s, 1H), 2.26 (s, 3H), 1.52-1.73 (m, 4H), 0.75- 0.97 (m, 6H). MS obsd. (ESI+) [(M+H)+]: 460.

Example 36-B was prepared in analogy to Example 1, Method A, Step 6 by using Compound 36g-B instead of 6-aminobenzyl(propylsulfonimidoyl)-7H-purinone (compound 1e). e 36-B(125 mg): 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.27 (d, J = 8 Hz, 2H), 7.14 (d, J = 8 Hz, 2H), 6.87 (br. s., 2H), 4.95 (s, 2H), 4.15 (s, 1H), 3.33-3.57 (m, 4H), 3.05 (s, 2H), 3.02 (s, 1H), 2.26 (s, 3H), 1.52-1.73 (m, 4H), 0.75-0.97 (m, 5H). MS obsd. (ESI+) +]: 460.

Example 37-A and Example 37-B 6-Amino[S(S)-propylsulfonimidoyl](p-tolylmethyl)(pyrrolidinecarbonyl)purin- 8-one and 6-amino[S(R)-propylsulfonimidoyl](p-tolylmethyl)(pyrrolidine carbonyl)purinone Example 37-A was prepared in analogy to Example 1, Method A, Step 6 by using Compound 36g-A and pyrrolidinecarbonyl chloride instead of 6-aminobenzyl (propylsulfonimidoyl)-7H-purinone (Compound 1e) and N-methyl-N-propyl-carbamoyl de mediate AA). e 37-A (390 mg) was obtained as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.31 - 7.11 (m, 4H), 7.04 (s, 2H), 4.95 (s, 2H), 4.15 (s, 1H), 3.65 - 3.47 (m, 4H), 3.37 (m, 2H), 2.27 (s, 3H), 1.97 - 1.81 (m, 4H), 1.71 - 1.59 (m, 2H), 0.94 (t, J = 7.4 Hz, 3H). MS obsd.

(ESI+) [(M+H)+]: 458.2.

Example 37-B (125 mg) was prepared in analogy to Example 37-A by using nd 36g-B instead of Compound 36g-A. 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.28 - 7.14 (m, 4H), 7.04 (s, 2H), 4.95 (s, 2H), 4.15 (s, 1H), 3.65 - 3.47 (m, 4H), 3.37 (m, 2H), 2.27 (s, 3H), 1.93 - 1.84 (m, 4H), 1.65 - 1.60 (m, 2H), 0.95 (t, J = 7.4 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 458.3.

Example 38-A and Example 38-B 6-Amino-N-(2-methoxyethyl)-N-methyloxo[S(S)-propylsulfonimidoyl](ptolylmethyl )purinecarboxamide and 6-amino-N-(2-methoxyethyl)-N-methyloxo [S(R)-propylsulfonimidoyl](p-tolylmethyl)purinecarboxamide O O NH2O N NH2O N N N N N HN O O O S N N S N N O HN Example 38-A was prepared in analogy to Example 1, Method A, Step 6 by using Compound 36g-A and N-(2-methoxyethyl)-N-methyl-carbamoyl chloride (Intermediate AB) instead of 6-aminobenzyl(propylsulfonimidoyl)-7H-purinone (Compound 1e) and N- methyl-N-propyl-carbamoyl chloride (Intermediate AA).

Example 38-A (57.8 mg) was obtained as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.26 (d, J = 7.6 Hz, 2H), 7.14 (d, J = 7.6 Hz, 2H), 6.89 - 6.78 (m, 2H), 4.95 (s, 2H), 4.18 (s, 1H), 3.62 -3.58 (m, 2H), 3.43 - 3.37 (m, 2H), 3.30 - 3.10 (m, 3H), 3.09 - 3.08 (m, 3H), 3.08 - 3.05 (m, 2H), 2.27 (s, 3H), 1.77 - 1.54 (m, 2H), 0.95 (t, J = 7.4 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 476.3.

Example 38-B (46.6 mg) was prepared in y to e 38-A by using Compound 36g-B instead of Compound 36g-A. 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.26 (d, J = 7.6 Hz, 2H), 7.14 (d, J = 7.6 Hz, 2H), 6.89 - 6.78 (m, 2H), 4.95 (s, 2H), 4.18 (s, 1H), 3.62 -3.58 (m, 2H), 3.43 - 3.37 (m, 2H), 3.30 - 3.10 (m, 3H), 3.09 - 3.08 (m, 3H), 3.08 - 3.05 (m, 2H), 2.27 (s, 3H), 1.77 - 1.54 (m, 2H), 0.95 (t, J = 7.4 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 476.3.

Example 39 6-Amino-N-ethyl-N-methyloxo(propylsulfonimidoyl)(p-tolylmethyl)purine carboxamide NH2 N O O S N N The title nd was prepared in analogy to Example 1, Method A, Step 6 by using N- ethyl-N-methyl-carbamoyl chloride and 6-amino(propylsulfonimidoyl)(p-tolylmethyl)-7H- purinone (Compound 36g) instead of N-methyl-N-propyl-carbamoyl chloride (Intermediate AA) and 6-aminobenzyl(propylsulfonimidoyl)-7H-purinone (Compound 1e). 6-Amino- N-ethyl-N-methyloxo(propylsulfonimidoyl)(p-tolylmethyl)purinecarboxamide (141.8 mg, Example 39) was obtained as a light yellow solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.26 (d, J = 7.9 Hz, 2H), 7.15 (d, J = 7.9 Hz, 2H), 6.89 (s, 2H), 4.95 (s, 2H), 4.24 - 4.07 (m, 1H), 3.52 - 3.35 (m, 4H), 3.10 - 2.95 (m, 3H), 2.26 (s, 3H), 1.77 - 1.55 (m, 2H), 1.24 - 1.10 (m, 3H), 0.95 (t, J = 7.4 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 446.1.

Example 40 6-Amino-N-butyl-N-methyloxo(propylsulfonimidoyl)(p-tolylmethyl)purine carboxamide The title nd was prepared in analogy to e 1, Method A, Step 6 by using 6- amino(propylsulfonimidoyl)(p-tolylmethyl)-7H-purinone (Compound 36g) and N- butyl-N-methyl-carbamoyl chloride instead of 6-aminobenzyl(propylsulfonimidoyl)-7H- purinone (Compound 1e) and N-methyl-N-propyl-carbamoyl chloride mediate AA). 6- Amino-N-butyl-N-methyloxo(propylsulfonimidoyl)(p-tolylmethyl)purine carboxamide (32 mg, Example 40) was obtained as a white solid. 1H NMR (400 MHz, DMSO- d6) δ ppm: 7.28 - 7.14 (m, 4H), 6.88 (s, 2H), 4.95 (s, 2H), 4.16 (s, 1H), 3.41 - 3.36 (m, 2H), 3.10 - 2.99 (m, 3H), 2.53 - 2.51 (m, 2H), 2.27 (s, 3H), 1.71 - 1.63 (m, 2H), 1.62 - 1.51 (m, 2H), 1.42 - 1.26 (m, 2H), 0.97 - 0.74 (m, 6H). MS obsd. (ESI+) [(M+H)+]: 474.3 Example 41-A and Example 41-B 6-Amino[(4-chlorophenyl)methyl][S(R)-ethylsulfonimidoyl]-N-methyloxo-N- propyl-purinecarboxamide (Example 41-A) and 6-Amino[(4-chlorophenyl)methyl] [S(S)-ethylsulfonimidoyl]-N-methyloxo-N-propyl-purinecarboxamide (Example 41-B) NH2O N HN O S N N 41-A 41-B Step 1: Preparation of 6-amino[(4-chlorophenyl)methyl]ethylsulfanyl-7H-purinone (Compound 41a) Compound 41a was prepared in analogy to Example 1, Method A, Step 3 by using iodoethane and 6-amino[(4-chlorophenyl)methyl]sulfanyl-7H-purinone (Compound 34b) instead of bromopropane and 6-aminophenylmethylsulfanyl-7H-purinone (Compound 1b). 6-Amino[(4-chlorophenyl)methyl]ethylsulfanyl-7H-purinone (2.5 g, nd 41a) was obtained as a white solid. MS obsd. (ESI+) +]: 336.

Step 2: Preparation of 6-amino(4-chlorobenzyl)ethylsulfinyl-7H-purinone (Compound 41b) S N N Compound 41b was ed in analogy to Example 1, Method A, Step 4 by using 6- amino[(4-chlorophenyl)methyl]ethylsulfanyl-7H-purinone (Compound 41a) instead of 6-aminobenzylpropylsulfanyl-7H-purinone (Compound 1c). 6-Amino(4- chlorobenzyl)ethylsulfinyl-7H-purinone (1.94 g, Compound 41b) was obtained as a white solid. MS obsd. (ESI+) [(M+H)+]: 352.

Step 3: Preparation of 6-amino[(4-chlorophenyl)methyl](ethylsulfonimidoyl)-7H- purinone (Compound 41c) O O S N N nd 41c was prepared in analogy to Example 1, Method A, Step 5 by using 6- 9-(4-chlorobenzyl)ethylsulfinyl-7H-purinone (Compound 41b) instead of 6-amino- 9-benzyl(2-methylsulfinyl)-7H-purinone (Compound 1d). 6-Amino[(4- chlorophenyl)methyl](ethylsulfonimidoyl)-7H-purinone (217 mg, Example 41c) was obtained as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 10.61 (s, 1H), 7.42 - 7.35 (m, 4H), 6.98 (s, 2H), 4.96 (s, 2H), 4.05 (s, 1H), 3.42 - 3.37 (m, 2H), 1.16 (t, J = 7.4 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 367.0.

Separation of compound of Compound 41c by chiral HPLC afforded Compound 41c-A (faster eluting, 31.8 mg) and Compound 41c-B (slower eluting, 10 mg) as white solid with ol 5%-40% (0.05%DEA)/CO2 on ChiralPak IC-3 column.

HN O S N N 41c-A Compound 41c-A: 1H NMR (400 MHz, DMSO-d6) δ ppm: 10.76 (s, 1H), 7.45 - 7.33 (m, 4H), 7.01 (s, 2H), 4.96 (s, 2H), 4.03 (s, 1H), 3.40 - 3.34 (m, 2H), 1.17 (t, J = 7.4 Hz, 3H). MS obsd.

(ESI+) [(M+H)+]: 367.0. 41c-B Compound 41c-B: 1H NMR (400 MHz, DMSO-d6) δ ppm: 10.70 (s, 1H), 7.46 -7.28 (m, 4H), 7.01 (s, 2H), 4.96 (s, 2H), 4.03 (s, 1H), 3.44 - 3.36 (m, 2H), 1.17 (t, J = 7.4 Hz, 3H). MS obsd.

(ESI+) [(M+H)+]: 367.0.

Step 4: 6-Amino[(4-chlorophenyl)methyl][S(R)-ethylsulfonimidoyl]-N-methyloxo- N-propyl-purinecarboxamide (Example 41-A) and 6-amino[(4-chlorophenyl)methyl]- 2-[S(S)-ethylsulfonimidoyl]-N-methyloxo-N-propyl-purinecarboxamide (Example 41- NH2O N NH2 N N N N N O O HN O S N N S N N HN O Cl Cl 41-A 41-B Example 41-A was prepared in analogy to Example 1, Method A, Step 6 by using Compound 41c-B d of 6-aminobenzyl(propylsulfonimidoyl)-7H-purinone (Compound 1e). 6-Amino[(4-chlorophenyl)methyl][S(R)-ethylsulfonimidoyl]-N-methyl- 8-oxo-N-propyl-purinecarboxamide (Example 41-A, 78 mg) was obtained as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.43 - 7.41 (m, 4H), 6.90 (s, 2H), 5.00 (s, 2H), 4.19 (s, 1H), 3.46-3.39 (m, 2H), 3.39 - 3.38 (m, 2H), 3.09-2.99 (m, 3H), 1.69 - 1.52 (m, 2H), 1.19 (t, J = 7.28 Hz, 3H), 0.95 - 0.66 (m, 3H). MS obsd. (ESI+) +]: 466.1.

Example 41-B (125 mg) was prepared in analogy to Example 1, Method A, Step 6 by using Compound 41c-A instead of 6-aminobenzyl(propylsulfonimidoyl)-7H-purinone (Compound 1e). 6-Amino[(4-chlorophenyl)methyl][S(S)-ethylsulfonimidoyl]-N-methyl oxo-N-propyl-purinecarboxamide (Example 41-B, 38 mg) was obtained as a white solid. 1H NMR (400 MHz, 6) δ ppm: 7.43 - 7.41 (m, 4H), 6.90 (s, 2H), 5.00 (s, 2H), 4.20 (s, 1H), 3.46 - 3.41 (m, 2H), 3.40 - 3.39 (m, 2H), 3.10 - 3.00 (m, 3H), 1.69 - 1.50 (m, 2H), 1.24 - 1.12 (m, 3H), 0.93 - 0.73 (m, 3H). (MS obsd. (ESI+) [(M+H)+]: 466.2.

The stereochemistry of Example 41-B was determined by single l X-ray diffraction shown in Figure 1.

Example 42-A and Example 42-B 6-Amino[(4-chlorophenyl)methyl]-N-ethyl-2[S(S)-ethylsulfonimidoyl]-N-methyloxopurinecarboxamide (Example 42-A) and 6-Amino[(4-chlorophenyl)methyl]-N-ethyl [S(R)-ethylsulfonimidoyl]-N-methyloxo-purinecarboxamide (Example 42-B) NH2O N O O S N N 42-A 42-B Example 42-A was prepared in analogy to Example 1, Method A, step 6 by using Compound 41c-A and N-ethyl-N-methyl-carbamoyl de instead of 6-aminobenzyl (propylsulfonimidoyl)-7H-purinone (Compound 1e) and N-methyl-N-propyl-carbamoyl chloride (Intermediate AA). 6-Amino[(4-chlorophenyl)methyl]-N-ethyl-2[S(S)- ethylsulfonimidoyl]-N-methyloxo-purinecarboxamide (Example 42-A, 40 mg) was obtained as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.43 - 7.41 (m, 4H), 6.90 (s, 2H), 4.99 (s, 2H), 4.18 (s, 1H), 3.48 - 3.40 (m, 2H), 3.39 (s, 2H), 3.05 – 3.01 (m, 3H), 1.20 - 1.14 (m, 6H). MS obsd. (ESI+) +]: 452.2.

Example 42-B was prepared in analogy to Example 1, Method A, Step 6 by using Compound 41c-B and N-ethyl-N-methyl-carbamoyl chloride instead of 6-aminobenzyl (propylsulfonimidoyl)-7H-purinone (Compound 1e) and N-methyl-N-propyl-carbamoyl de (Intermediate AA). 6-Amino[(4-chlorophenyl)methyl]-N-ethyl[S(R)- ethylsulfonimidoyl]-N-methyloxo-purinecarboxamide (Example 42-B, 38 mg) was obtained as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.43 - 7.41 (m, 4H), 6.91 (s, 2H), 4.98 (s, 2H), 4.19 (s, 1H), 3.48 - 3.40 (m, 2H), 3.39 (s, 2H), 3.09 - 2.97 (m, 3H), 1.23 - 1.11 (m, 6H). MS obsd. (ESI+) [(M+H)+]: 452.2.

The stereochemistry of Example 42-A was determined by single crystal X-ray diffraction shown in Figure 2.

Example 43-A and Example 43-B 6-Amino[S(R)-ethylsulfonimidoyl]-N-methyloxo-N-propyl(p-tolylmethyl)purine carboxamide le 43-A) and 6-Amino[S(S)-ethylsulfonimidoyl]-N-methyloxo-N- propyl(p-tolylmethyl)purinecarboxamide (Example 43-B) NH2O N NH2O N N N O N HN O S N N HN S N N 43-A 43-B Step 1: Preparation of ooxo(p-tolylmethyl)-1H-imidazolecarbonitrile (Compound 43a) Compound 43a was prepared in analogy to Example 1, Method A, Step 1 by using 4- methylbenzyl isocyanate instead of benzyl isocyanate. 4-Aminooxo(p-tolylmethyl)-1H- olecarbonitrile (26.6 g, Compound 43a) was obtained as a grey solid and used ly for next step without further purification. MS obsd. (ESI+) [(M+H)+]: 229.2.

Step 2: Preparation of 6-amino(p-tolylmethyl)sulfanyl-7H-purinone (Compound HS N N Compound 43b was prepared in analogy to Example 1, Method A, Step 2 by using of 4- aminooxo(p-tolylmethyl)-1H-imidazolecarbonitrile (compound 43a) instead of 4- aminobenzyloxo-1H-imidazolecarbonitrile (Compound 1a). 6-Amino(ptolylmethyl )sulfanyl-7H-purinone (20.0 g, nd 43b) was obtained as a yellow solid.

MS obsd. (ESI+) [(M+H)+]: 288.

Step 3: Preparation of 6-aminoethylsulfanyl(p-tolylmethyl)-7H-purinone (Compound 43c) Compound 43c was prepared in analogy to Example 1, Method A, Step 3 by using 6- amino(p-tolylmethyl)sulfanyl-7H-purinone und 43b) and iodoethane instead of 6-aminobenzylsulfanyl-7H-purinone (Compound 1b) and bromopropane. 6-Amino ethylsulfanyl(p-tolylmethyl)-7H-purinone (13 g, Compound 43c) was obtained as a yellow solid. MS obsd. (ESI+) [(M+H)+]: 316.

Step 4: Preparation of 6-aminoethylsulfinyl(p-tolylmethyl)-7H-purinone und 43d) N N S N N Compound 43d was prepared in analogy to Example 1, Method A, Step 4 by using 6- aminoethylsulfanyl(p-tolylmethyl)-7H-purinone (Compound 43c) instead of 6-amino- 9-benzylmethylsulfanyl-7H-purinone und 1c). 6-Aminoethylsulfinyl(ptolylmethyl )-7H-purinone6 (3.5 g, Compound 43d) was obtained as a yellow solid. MS obsd.

(ESI+) [(M+H)+]: 332.

Step 5: Preparation of 6-amino(ethylsulfonimidoyl)(p-tolylmethyl)-7H-purinone (Compound 43e) Compound 43e was prepared in y to Example 1, Method A, Step 5 by using 6- aminoethylsulfinyl(p-tolylmethyl)-7H-purinone und 43d) instead of 6-amino- 9-benzylmethylsulfinyl-7H-purinone (Compound 1d). 6-Amino(ethylsulfonimidoyl) (p-tolylmethyl)-7H-purinone (530 mg, Compound 43e) was obtained as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 10.53 (s, 1H), 7.24 (d, J = 8.03 Hz, 2H), 7.13 (d, J = 8.03 Hz, 2H), 6.94 (br. s., 2H), 4.91 (s, 2H), 4.03 (s, 1H), 3.36 - 3.41 (m, 2H), 2.26 (s, 3H), 1.18 (t, J = 7.28 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 347.

Separation of compound of Compound 43e by chiral HPLC afforded Compound 43e-A (faster eluting, 56.8 mg) and Compound 43e-B (slower eluting, 56.7 mg) as white solid with methanol 5%-40% (0.05%DEA)/CO2 on ChiralPak AD-3 column. 43e-A Compound 43e-A: 1H NMR (400 MHz, 6) δ ppm: 10.52 (br. s., 1H), 7.23 (d,J = 8.0 Hz, 2H), 7.13 (d, J = 7.9 Hz, 2H), 6.94 (br. s., 2H), 4.90 (s, 2H), 4.03 (s, 1H), 3.42 - 3.33 (m, 2H), 2.25 (s, 3H), 1.17 (t, J = 7.3 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 347.

HN O S N N 43e-B Compound 43e-B: 1H NMR (400 MHz, DMSO-d6) δ ppm: 10.56 (br. s., 1H), 7.23 (d, J = 8.0 Hz, 2H), 7.13 (d, J = 8.0 Hz, 2H), 6.95 (br. s., 2H), 4.90 (s, 2H) 4.03 (s, 1H), 3.44 - 3.29 (m, 2H), 2.25 (s, 3H), 1.17 (t, J = 7.3 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 347.

Step 6: Preparation of 6-Amino[S(R)-ethylsulfonimidoyl]-N-methyloxo-N-propyl (p-tolylmethyl)purinecarboxamide (Example 43-A) and 6-Amino[S(S)- ethylsulfonimidoyl]-N-methyloxo-N-propyl(p-tolylmethyl)purinecarboxamide (Example 43-B) NH2O N O O S N N 43-A 43-B Example 43-A was ed in analogy to e 1, Method A, Step 6 by using Compound 43e-A instead of 6-aminobenzyl(propylsulfonimidoyl)-7H-purinone (Compound 1e). 6-Amino[S(R)-ethylsulfonimidoyl]-N-methyloxo-N-propyl(ptolylmethyl ecarboxamide (Example 43-A, 58.1 mg, faster eluting, isopropanol from % to 40% (0.05%DEA)/CO2 on ChiralPak AD-3 column) was obtained as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.28 (d, J = 7.8 Hz, 2H), 7.15 (d, J = 7.8 Hz, 2H), 6.88 (br. s., 2H), 5.03 - 4.87 (m, 2H), 4.19 (s, 1H), 3.61 - 3.36 (m, 4H), 3.11 – 2.96 (m, 3H), 2.26 (s, 3H), 1.72 - 1.45 (m, 2H), 1.20 (t, J = 7.2 Hz, 3H), 0.97 - 0.65 (m, 3H). MS obsd. (ESI+) [(M+H)+]: Example 43-B was prepared in analogy to Example 1, Method A, Step 6 by using nd 43e-B instead of 6-aminobenzyl(propylsulfonimidoyl)-7H-purinone (Compound 1e). 6-Amino[S(S)-ethylsulfonimidoyl]-N-methyloxo-N-propyl(ptolylmethyl )purinecarboxamide (Example 43-B, 40.1 mg, slower eluting, isopropanol from % to 40% (0.05%DEA)/CO2 on ChiralPak AD-3 column) was obtained as a white solid: 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.28 (d, J = 7.5 Hz, 2H), 7.15 (d, J = 7.5 Hz, 2H), 6.89 (br. s., 2H), 5.03 - 4.86 (m, 2H), 4.19 (s, 1H), 3.49 - 3.37 (m, 4H), 3.08 - 3.00 (m, 3H), 2.27 (s, 3H), 1.70 - 1.48 (m, 2H), 1.20 (t, J = 7.2 Hz, 3H), 0.95 - 0.71 (m, 3H). MS obsd. (ESI+) [(M+H)+]: 446.3.

The stereochemistry of Example 43-B was determined by single crystal X-ray diffraction shown in Figure 3.

Example 44-A and Example 44-B 6-Amino-N-ethyl-2[S(S)-ethylsulfonimidoyl]-N-methyloxo(p-tolylmethyl)purine carboxamide (Example 44-A) and 6-Amino-N-ethyl[S(R)-ethylsulfonimidoyl]-N-methyl- 8-oxo(p-tolylmethyl)purinecarboxamide (Example 44-B) 44-A 44-B Example 44-A was ed in analogy to Example 1, Method A, Step 6 by using Compound 43e-B and N-ethyl-N-methyl-carbamoyl chloride instead of 6-aminobenzyl (propylsulfonimidoyl)-7H-purinone und 1e) and N-methyl-N-propyl-carbamoyl de (Intermediate AA). 6-Amino-N-ethyl-2[S(S)-ethylsulfonimidoyl]-N-methyloxo (p-tolylmethyl)purinecarboxamide (Example 44-A, 73.1 mg) was obtained as a white solid. 1H NMR (400 MHz, DMSO-d δ ppm: 7.28 (d, J = 7.8 Hz, 2H), 7.15 (d, J = 7.8 Hz, 2H), 6.90 (br. s., 2H), 4.95 (s, 2H), 4.19 (br. s., 1H), 3.48 - 3.39 (m, 4H), 3.06 - 3.00 (m, 3H), 2.27 (s, 3H), 1.29 - 1.04 (m, 6H). MS obsd. (ESI+) [(M+H)+]: 432.

Example 44-B was prepared in analogy to Example 1, Method A, Step 6 by using Compound 43e-A and N-ethyl-N-methyl-carbamoyl chloride d of 6-aminobenzyl lsulfonimidoyl)-7H-purinone (Compound 1e) and N-methyl-N-propyl-carbamoyl chloride (Intermediate AA). 6-Amino-N-ethyl[S(R)-ethylsulfonimidoyl]-N-methyloxo (p-tolylmethyl)purinecarboxamide (Example 44-B, 46.7 mg) was obtained as a white solid: 1H NMR (400 MHz, DMSO-d 6) δ ppm: 7.28 (d, J = 7.9 Hz, 2H), 7.15 (d, J = 7.9 Hz, 2H), 6.90 (br. s., 2H), 4.95 (s, 2H), 4.19 (br. s., 1H), 3.50 - 3.39 (m, 4H), 3.10 – 2.96 (m, 3H), 2.27 (s, 3H), 1.27 - 1.10 (m, 6H). MS obsd. (ESI+) [(M+H)+]: 432.

Example 45-A and Example 45-B 6-Amino[S(R)ethylsulfonimidoyl][(4-fluorophenyl)methyl]-N-methyloxo-N-propyl- purinecarboxamide and 6-Amino[S(S)ethylsulfonimidoyl][(4-fluorophenyl)methyl]- N-methyloxo-N-propyl-purinecarboxamide NH2O N O O S N N Step 1: Preparation of 4-amino[(4-fluorophenyl)methyl]oxo-1H-imidazole itrile (Compound 45a) nd 45a was prepared in analogy to Example 1, Method A, Step 1 by using 4- fluorobenzyl isocyanate instead of benzyl isocyanate. 4-Amino[(4-fluorophenyl)methyl] oxo-1H-imidazolecarbonitrile (48 g, Compound 45a) was obtained as a light yellow solid and was used directly for next step without further purification. MS obsd. (ESI+) [(M+H)+]: 233.

Step 2: Preparation of 6-amino[(4-fluorophenyl)methyl]sulfanyl-7H-purinone (Compound 45b) HS N N Compound 45b was prepared in y to Example 1, Method A, Step 2 by using of 4- amino[(4-fluorophenyl)methyl]oxo-1H-imidazolecarbonitrile (Compound 45a) instead of 4-aminophenylmethyloxo-1H-imidazolecarbonitrile (Compound 1a). 6-Amino [(4-fluorophenyl)methyl]sulfanyl-7H-purinone (32.0 g, Compound 45b) was obtained as a yellow solid. MS obsd. (ESI+) [(M+H)+]: 292.

Step 3: Preparation of 6-aminoethylsulfanyl[(4-fluorophenyl)methyl]-7H-purinone (Compound 45c) Compound 45c was prepared in analogy to Example 1, Method A, Step 3 by using 6- amino[(4-fluorophenyl)methyl]sulfanyl-7H-purinone (Compound 45b) and hane instead of 6-aminobenzylsulfanyl-7H-purinone (Compound 1b) and bromopropane. 6- Aminoethylsulfanyl[(4-fluorophenyl)methyl]-7H-purinone (5.6 g, Compound 45c) was obtained as a yellow solid. MS obsd. (ESI+) [(M+H)+]: 320.

Step 5: Preparation of oethylsulfinyl[(4-fluorophenyl)methyl]-7H-purinone (Compound 45d) Compound 45d was prepared in analogy to Example 1, Method A, Step 4 by using 6- aminoethylsulfanyl[(4-fluorophenyl)methyl]-7H-purinone (Compound 45c) instead of 6-aminobenzylpropylsulfanyl-7H-purinone (Compound 1c). 6-Aminoethylsulfinyl- 9-[(4-fluorophenyl)methyl]-7H-purinone (4.8 g, nd 45d) was obtained as a yellow solid. MS obsd. (ESI+) [(M+H)+]: 332.

Step 6: Preparation of 6-amino(ethylsulfonimidoyl)[(4-fluorophenyl)methyl]-7H- 8-one (Compound 45e) Compound 45e was prepared in analogy to Example 1, Method A, Step 5 by using 6- aminoethylsulfinyl[(4-fluorophenyl)methyl]-7H-purinone (Compound 45d) instead of 6-aminobenzylpropylsulfinyl-7H-purinone (Compound 1d). 6-Amino (ethylsulfonimidoyl)[(4-fluorophenyl)methyl]-7H-purinone (2.9 g, Compound 45e) was ed as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 10.57 (br. s., 1H), 7.40 (dd, J = 8.5, 5.5 Hz, 2H), 7.16 (t, J = 8.9 Hz, 2H), 6.97 (br. s., 2H), 4.94 (s, 2H), 4.07 (s, 1H), 3.43 - 3.36 (m, 2H), 1.17 (t, J = 7.4 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 351.

Separation of compound of Compound 45e by chiral HPLC afforded Compound 45e-A (faster eluting, 85.4 mg) and Compound 45e-B (slower eluting, 36.4 mg) as white solid with ol 5%-40% (0.05%DEA)/CO2 on ChiralPak AD-3 column.

Compound 45e-A: 1H NMR (400 MHz, DMSO-d6) δ ppm: 10.53 (br. s., 1H), 7.41 (dd, J = 8.5, .5 Hz, 2H), 7.17 (t, J = 8.9 Hz, 2H), 6.98 (br. s., 2H), 4.95 (s, 2H), 4.07 (s, 1H), 3.45 - 3.36 (m, 2H), 1.17 (t, J = 7.3 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 351.

Compound 45e-B: 1H NMR (400 MHz, DMSO-d6) δ ppm: 10.53 (br. s., 1H), 7.41 (dd, J = 8.5, .5 Hz, 2H), 7.17 (t, J = 8.9 Hz, 2H), 6.98 (br. s., 2H), 4.95 (s, 2H), 4.07 (s, 1H), 3.44 - 3.37 (m, 2H) 1.17 (t, J = 7.3 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 351.

Step 7: Preparation of 6-amino(ethylsulfonimidoyl)[(4-fluorophenyl)methyl]-N- methyloxo-N-propyl-purinecarboxamide (Example 45), 6-Amino [S(R)ethylsulfonimidoyl][(4-fluorophenyl)methyl]-N-methyloxo-N-propyl-purine carboxamide and o[S(S)ethylsulfonimidoyl][(4-fluorophenyl)methyl]-N- methyloxo-N-propyl-purinecarboxamide (Example 45-A and Example 45-B).

(Example 45) NH2O N O O S N N (Example 45-A and Example 45-B) Example 45 was prepared in analogy to Example 1, Method A, Step 6 by using o- 2-(ethylsulfonimidoyl)[(4-fluorophenyl)methyl]-7H-purinone (Compound 45e) instead of obenzyl(propylsulfonimidoyl)-7H-purinone (Compound 1e). 6-Amino (ethylsulfonimidoyl)[(4-fluorophenyl)methyl]-N-methyloxo-N-propyl-purine carboxamide (162.4 mg, Example 45) was obtained as a white solid.

Separation of compound of Example 45 by chiral HPLC afforded Example 45-A (faster eluting, 85.3 mg) and Example 45-B (slower g, 52 mg) as white solid with methanol 5%- 40% (0.05%DEA)/CO2 on ChiralPak AD-3 column Example 45-A: 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.53 - 7.38 (m, 2H), 7.18 (t, J = 8.9 Hz, 2H), 6.90 (br. s., 2H), 4.99 (s, 2H), 4.21 (s, 1H), 3.48 - 3.37 (m, 4H), 3.10 - 3.01 (m, 3H), 1.69 - 1.49 (m, 2H), 1.25 - 1.14 (m, 3H), 0.94 - 0.72 (m, 3H). MS obsd. (ESI+) [(M+H)+]: 450.

Example 45-B: 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.54 - 7.38 (m, 2H), 7.18 (t, J = 8.9 Hz, 2H), 7.01 - 6.72 (m, 2H), 4.99 (s, 2H), 4.21 (s, 1H), 3.46 - 3.38 (m, 4H), 3.10 - 3.01 (m, 3H), 1.76 - 1.50 (m, 2H), 1.25 - 1.16 (m, 3H), 0.99 - 0.69 (m, 3H). MS obsd. (ESI+) [(M+H)+]: 450.

Example 46-A and Example 46-B 6-Amino-N-ethyl(ethylsulfonimidoyl)[(4-fluorophenyl)methyl]-N-methyloxopurinecarboxamide (Example 46), o-N-ethyl[S(S)-(ethylsulfonimidoyl)][(4- phenyl)methyl]-N-methyloxo-purinecarboxamide and 6-amino-N-ethyl[S(R)- (ethylsulfonimidoyl)][(4-fluorophenyl)methyl]-N-methyloxo-purinecarboxamide (Example 46-A and Example 46-B).

(Example 46) (Example 46-A and Example 46-B) Example 46 was prepared in analogy to Example 1, Method A, Step 6 by using 6-amino- 2-(ethylsulfonimidoyl)[(4-fluorophenyl)methyl]-7H-purinone (Compound 45e) and N- ethyl-N-methyl carbamoyl chloride d of 6-aminobenzyl(propylsulfonimidoyl)-7H- purinone (Compound 1e) and N-methyl-N-propyl-carbamoyl chloride (Intermediate AA). 6- Amino-N-ethyl(ethylsulfonimidoyl)[(4-fluorophenyl)methyl]-N-methyloxo-purine carboxamide (51 mg, Example 46) was obtained as a white solid. 1H NMR (400 MHz, DMSO- d6) δ ppm: 7.46 - 7.43 (m, 2H), 7.20-7.15 (m, 2H), 6.90 (br. s., 2H), 4.98 (s, 2H), 4.18 (s, 1H), 3.47 - 3.32 (m, 4H), 3.05 - 3.01 (m, 3H), 1.21 - 1.14 (m, 6H). MS obsd. (ESI+) [(M+H)+]: 436. tion of compound of Example 46 by chiral HPLC afforded Example 46-A (faster eluting, 72 mg) and Example 46-B (slower eluting, 45 mg) as white solid with methanol 5%- 40% (0.05%DEA)/CO2 on ChiralPak AD-3 column Example 46-A: 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.46 - 7.43 (m, 2H), 7.20-7.16 (m, 2H), 6.90 (br. s., 2H), 4.98 (s, 2H), 4.18 (s, 1H), 3.47 - 3.32 (m, 4H), 3.05 - 3.01 (m, 3H), 1.21- 1.14 (m, 6H). MS obsd. (ESI+) [(M+H)+]: 436.

Example 46-B: 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.46 - 7.43 (m, 2H), 7.20-7.14 (m, 2H), 6.92 (br. s., 2H), 4.98 (s, 2H), 4.20 (br. s., 1H), 3.47 - 3.32 (m, 4H), 3.05 - 3.01 (m, 3H), 1.23 - 1.19 (m, 6H). MS obsd. (ESI+) [(M+H)+]: 436.

Example 47-A and Example 47-B 6-Amino[(4-bromophenyl)methyl](ethylsulfonimidoyl)-N-methyloxo-N-propyl- carboxamide (Example 47), 6-amino[S(R)-ethylsulfonimidoyl][(4- bromophenyl)methyl]-N-methyloxo-N-propyl-purinecarboxamide and o [S(S)-ethylsulfonimidoyl][(4-bromophenyl)methyl]-N-methyloxo-N-propyl-purine carboxamide NH2O N O O S N N (Example 47) (Example 47-A and Example 47-B) Step 1: Preparation of 4-amino[(4-bromophenyl)methyl]oxo-1H-imidazole carbonitrile (Compound 47a) Compound 47a was prepared in analogy to Example 1, Method A, Step 1 by using 4- bromobenzyl isocyanate instead of benzyl isocyanate. 4-Amino[(4-bromophenyl)methyl] oxo-1H-imidazolecarbonitrile (500 mg, Compound 47a) was obtained as a light yellow solid and was used directly for next step without further purification. 1H NMR (400 MHz, 6) δ ppm: 9.94 (S, 1H), 7.55-7.53 (d, J = 8.0 Hz, 2H), 7.20-7.18 (d, J = 8.0 Hz, 2H), 6.52 (br. s., 2H), 4.74 (s, 2H). MS obsd. (ESI+) [(M+H)+]: 293.

Step 2: Preparation of 6-amino[(4-bromophenyl)methyl]sulfanyl-7H-purinone (Compound 47b) N N HS N N Compound 47b was prepared in analogy to Example 1, Method A, Step 2 by using of 4- amino[(4-bromophenyl)methyl]oxo-1H-imidazolecarbonitrile (Compound 47a) instead of 4-aminophenylmethyloxo-1H-imidazolecarbonitrile (Compound 1a). 6-Amino [(4-bromophenyl)methyl]sulfanyl-7H-purinone (300 mg, Compound 47b) was ed as a yellow solid. MS obsd. (ESI+) [(M+H)+]: 352.

Step 3: Preparation of 6-aminoethylsulfanyl[(4-bromophenyl)methyl]-7H-purinone (Compound 47c) N N S N N 47c Compound 47c was prepared in analogy to Example 1, Method A, Step 3 by using 6- 9-[(4-bromophenyl)methyl]sulfanyl-7H-purinone (Compound 45b) and iodoethane instead of 6-aminobenzylsulfanyl-7H-purinone (Compound 1b) and ropane. 6- Aminoethylsulfanyl[(4-bromophenyl)methyl]-7H-purinone (5.6 g, Compound 47c) was obtained as a yellow solid. MS obsd. (ESI+) [(M+H)+]: 380.

Step 4: Preparation of 6-amino[(4-bromophenyl)methyl]ethylsulfinyl-7H-purinone (Compound 47d) Compound 47d was prepared in analogy to Example 1, Method B, Step 6 by using 6- amino[(4-bromophenyl)methyl]ethylsulfanyl-7H-purinone ( nd 47c) instead of obenzyl(2-propylsulfanyl)-7H-purinone (Compound 1c). 6-Amino[(4- bromophenyl)methyl]ethylsulfinyl-7H-purinone (3.2 g, Compound 47d) was obtained as a white solid. MS obsd. (ESI+) [(M+H)+]: 396.

Step 5: Preparation of 6-amino[(4-bromophenyl)methyl](ethylsulfonimidoyl)-7H- purinone (Compound 47e) Compound 47e was prepared in y to Example 1, Method B, Step 7 by using 6- amino[(4-bromophenyl)methyl]ethylsulfinyl-7H-purinone (Compound 47d) instead of 6-aminobenzylpropylsulfinyl-7H-purinone (Compound 1d). 6-Amino[(4- bromophenyl)methyl](ethylsulfonimidoyl)-7H-purinone (4.0 g, Compound 47e) was obtained as a white solid. MS obsd. (ESI+) [(M+H)+]: 411. nd 47e-A and nd 47e-B Separation of compound of Compound 47e by chiral HPLC afforded Compound 47e-A (faster eluting, 112 mg) and Compound 47e-B (slower eluting, 99 mg) as white solid with methanol 5%-40% (0.05%DEA)/CO2 on ChiralPak AD-3 column.

Compound 47e-A: 1H NMR (400 MHz, DMSO-d6) δ ppm: 10.58 (br. s., 1H), 7.52-7.54 (d, J = 8.0, 2H), 7.31-7.29 (t, J = 8.0 Hz, 2H), 6.54 (br. s., 2H), 4.93 (s, 2H), 4.05 (s, 1H), 3.42 - 3.31 (m, 2H), 1.15 (t, J = 7.3 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 411.

Compound 47e-B: 1H NMR (400 MHz, DMSO-d6) δ ppm: 10.58 (br. s., 1H), 7.54-7.52 (d, J = 8.0, 2H), 7.31-7.29 (t, J = 8.0 Hz, 2H), 6.98 (br. s., 2H), 4.93 (s, 2H), 4.06 (s, 1H), 3.40 - 3.37 (m, 2H), 1.15 (t, J = 7.3 Hz, 3H). MS obsd. (ESI+) [(M+H)+]: 411.

Step 6: Preparation of 6-amino[(4-bromophenyl)methyl](ethylsulfonimidoyl)-N- methyloxo-N-propyl-purinecarboxamide (Example 47), 6-amino[(4- bromophenyl)methyl][S(R)-ethylsulfonimidoyl]-N-methyloxo-N-propyl-purine carboxamide and 6-amino[(4-bromophenyl)methyl][S(S)-ethylsulfonimidoyl]-N- oxo-N-propyl-purinecarboxamide (Example 47-A and Example 47-B).

(Example 47) NH2O N HN O S N N (Example 47-A and Example 47-B) Example 47 was prepared in analogy to e 1, Method A, Step 6 by using 6-amino- 9-[(4-bromophenyl)methyl](ethylsulfonimidoyl)-7H-purinone (Compound 47e) instead of 6-aminobenzyl(propylsulfonimidoyl)-7H-purinone (Compound 1e). 6-Amino[(4- bromophenyl)methyl](ethylsulfonimidoyl)-N-methyloxo-N-propyl-purinecarboxamide (570 mg, e 47) was obtained as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.56 - 7.53 (m, 2H), 7.36-7.34 (m, 2H), 6.92 (br. s., 2H), 4.97 (s, 2H), 4.18 (s, 1H), 3.45 - 3.38 (m, 4H), 3.05 - 3.02 (m, 3H), 1.65-1.56 (m, 2H), 1.19 (t, J = 8.0 Hz, 3H), 0.93-0.75 (m, 3H). MS obsd. (ESI+) [(M+H)+]: 510. tion of compound of Example 47 by chiral HPLC afforded Example 47-A (faster eluting, 260 mg) and Example 47-B (slower eluting, 266 mg) as white solid with methanol 5%- 40% (0.05%DEA)/CO2 on ChiralPak AD-3 column Example 47-A: 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.56 - 7.54 (d, J = 8.0 Hz, 2H), 7.36-7.33 (d, J = 8,0 Hz, 2H), 6.90 (br. s., 2H), 4.97 (s, 2H), 4.21 (s, 1H), 3.46 - 3.41 (m, 4H), 3.05 - 3.02 (m, 3H),1.65-1.54 (m, 2H), 1.24-1.16 (m, 3H), 0.93-0.75 (m, 3H). MS obsd. (ESI+) [(M+H)+]: 510.

Example 47-B: 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.54 - 7.53 (d, J = 8.0 Hz, 2H), 7.36-7.33 (d, J = 8,0 Hz, 2H), 6.90 (br. s., 2H), 4.97 (s, 2H), 4.21 (s, 1H), 3.46 - 3.41 (m, 4H), 3.06 - 3.02 (m, 3H), 1.65-1.54 (m, 2H), 1.20-1.16 (m, 3H), 0.93-0.75 (m, 3H). MS obsd. (ESI+) [(M+H)+]: 510.

Example 48-A and Example 48-B 6-Amino[(4-bromophenyl)methyl]-N-ethyl(ethylsulfonimidoyl)-N-methyloxopurinecarboxamide (Example 48), 6-amino[(4-bromophenyl)methyl]-N-ethyl[S(S)- sulfonimidoyl)]-N-methyloxo-purinecarboxamide and 6-amino[(4- bromophenyl)methyl]-N-ethyl[S(R)-(ethylsulfonimidoyl)]-N-methyloxo-purine carboxamide (Example 48-A and Example 48-B).

(Example 48) NH2 N N N O O S N N (Example 48-A and Example 48-B) Example 48 was prepared in analogy to Example 1, Method A, Step 6 by using 6-amino- 9-[(4-bromophenyl)methyl](ethylsulfonimidoyl)-7H-purinone (Compound 47e) and N- ethyl-N-methyl-carbamoyl chloride instead of 6-aminobenzyl(propylsulfonimidoyl)-7H- purinone (Compound 1e) and N-methyl-N-propyl-carbamoyl chloride (Intermediate AA). 6- Amino[(4-bromophenyl)methyl](ethylsulfonimidoyl)-N-methyloxo-N-propyl-purine carboxamide (469 mg, Example 48) was ed as a white solid. 1H NMR (400 MHz, DMSO- d6) δ ppm: 7.56 - 7.54 (d, J = 8.0 Hz, 2H), 7.36-7.34 (d, J = 8,0 Hz, 2H), 6.98 (br. s., 2H), 4.97 (s, 2H), 3.53 - 3.46 (m, 4H), 3.05 - 3.01 (m, 3H), 1.22-1.16 (m, 6H). MS obsd. (ESI+) [(M+H)+]: 496.

Separation of compound of Example 48 by chiral HPLC ed Example 48-A (faster eluting, 198 mg) and e 48-B (slower eluting, 202 mg) as white solid with methanol 5%- 40% (0.05%DEA)/CO2 on ChiralPak AD-3 column.

Example 48-A: 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.56 - 7.54 (d, J = 8.0 Hz, 2H), 7.36-7.34 (d, J = 8,0 Hz, 2H), 6.92 (br. s., 2H), 4.97 (s, 2H), 4.19 - 4.18 (m, 1H), 3.46 - 3.41 (m, 4H), 3.05 - 3.01 (m, 3H), .14 (m, 6H). MS obsd. (ESI+) [(M+H)+]: 496.

Example 48-B: 1H NMR (400 MHz, DMSO-d6) δ ppm: 7.56 - 7.54 (d, J = 8.0 Hz, 2H), 7.36-7.34 (d, J = 8,0 Hz, 2H), 6.92 (br. s., 2H), 4.97 (s, 2H), 4.24 (br. s., 1H), 3.58 - 3.41 (m, 4H), 3.05 - 3.01 (m, 3H), 1.26-1.01 (m, 6H). MS obsd. (ESI+) +]: 496.

Example 49 Activity of Compounds and Examples in HEK293-hTLR-7 assay HEK293-Blue-hTLR-7 cells assay: A stable HEK293-Blue-hTLR-7 cell line was purchased from InvivoGen (Cat.#: hkb-htlr7, San Diego, California, USA). These cells were designed for studying the stimulation of human TLR7 by monitoring the activation of NF-κB. A SEAP (secreted embryonic alkaline phosphatase) reporter gene was placed under the control of the IFN-β minimal promoter fused to five NF-κB and APbinding sites. The SEAP was induced by activating NF-κB and AP-1 via stimulating HEK-Blue hTLR7 cells with TLR7 ligands. ore the reporter expression was regulated by the NF-κB promoter upon stimulation of human TLR7 for 20 hrs. The cell culture supernatant SEAP reporter activity was determined using QUANTI-Blue™ kit (Cat.#: rep-qb1, Invivogen, San Diego, Ca, USA) at a wavelength of 640 nm, a detection medium that turns purple or blue in the ce of alkaline phosphatase.

HEK293-Blue-hTLR7 cells were incubated at a y of 250,000~450,000 cells/mL in a volume of 180 µL in a 96-well plate in Dulbecco's Modified Eagle's medium (DMEM) containing 4.5 g/L glucose, 50 U/mL penicillin, 50 mg/mL streptomycin, 100 mg/mL Normocin, 2 mM L-glutamine, 10% (V/V) nactivated fetal bovine serum for 24 hrs. Then the HEK293-Blue-hTLR-7 cells were incubated with addition of 20 µL test compound in a serial dilution in the presence of final DMSO at 1% and m incubation under 37 ºC in a CO2 incubator for 20 hrs. Then 20 µL of the supernatant from each well was incubated with 180 µL -blue substrate solution at 37oC for 2 hrs and the absorbance was read at 620~655 nm using a spectrophotometer. The signalling pathway that TLR7 activation leads to downstream NF-κB activation has been widely accepted, and therefore similar reporter assay was also widely used for evaluating TLR7 t (Tsuneyasu Kaisho and Takashi Tanaka, Trends in Immunology, Volume 29, Issue 7, July 2008, Pages 329.sci; Hiroaki Hemmi et al, Nature Immunology 3, 196 - 200 (2002)).

The Compounds and Examples of the present invention were tested in HEK293- hTLR-7 assay for their TLR7 agonism ty as described herein and results are listed in Table 1. The es of prodrugs were found to have EC50 of about 2.1 µM to about 1000 µM, the Compounds of active forms were found to have EC50 less than 0.2 µM. The calculated ratio of EC50(prodrug) / EC50(active form) were within the range from 32 to about 7600.

Table 1. Activity of Examples and Compounds of present invention in -hTLR-7 assay HEK293- Ratio Corresponding hTLR-7 EC50 Prodrug hTLR-7 EC50 (EC50(prodrug) / Active Form (Active form, (Prodrug, µM) EC50(active form)) Example 1 50.4 Compound 1e 0.065 775.4 Example 1-A 42.5 Compound 1e-A 0.067 634.3 Example 1-B 27 Compound 1e-B 0.086 314.0 Example 2 32 nd 1e 0.065 372.1 Example 2-A 3.7 Compound 1e-B 0.086 43.0 Example 2-B 4.4 Compound 1e-A 0.067 65.7 Example 3 15.1 Compound 1e 0.065 232.3 e 4 23 Compound 1e 0.065 353.8 Example 5 41 Compound 1e 0.065 630.8 Example 6 82.3 Compound 1e 0.065 1266.2 Example 7 19.9 Compound 1e 0.065 306.2 Example 8 2.1 Compound 1e 0.065 32.3 Example 9 19.2 Compound 1e 0.065 295.4 Example 10 68.5 Compound 1e 0.065 1053.8 Example 11 5.6 Compound 1e 0.065 86.2 Example 12 43.9 Compound 1e 0.065 675.4 Example 13 67 Compound 1e 0.065 1030.8 Example 14 2.4 Compound 1e 0.065 36.9 Example 15 494 Compound 1e 0.065 7600 Example 16 32.1 Compound 1e 0.065 493.8 e 25 24.2 Compound 1e 0.065 372.3 Example 26 13.4 Compound 1e 0.065 206.2 Example 27 31.7 Compound 1e 0.065 487.7 Example 28 6.9 Compound 1e 0.065 106.2 Example 29 48.8 Compound 1e 0.065 750.8 Example 32 22.5 nd 1e 0.065 346.2 Example 34-A 6.0 Compound 34e-A 0.014 428.6 Example 34-B 6.36 Compound 34e-B 0.011 578.2 Example 36-A 31.8 Compound 36g-A 0.019 1673.7 Example 37-A 26.6 Compound 36g-A 0.019 1400 Example 37-B 47.4 Compound 36g-B 0.022 2154.5 Example 38-A 26.2 nd 36g-A 0.019 1378.9 Example 38-B 19.5 Compound 36g-B 0.022 886.4 Example 39 4.3 Compound 36g 0.027 159.3 Example 40 52.8 Compound 36g 0.027 1955.6 e 41 36 Compound 41c 0.053 679.2 Example 41-A 44.1 Compound 41c-B 0.085 518.8 Example 41-B 32.1 nd 41c-A 0.071 452.1 Example 42-A 40.5 Compound 41c-A 0.071 570.4 Example 42-B 49.2 Compound 41c-B 0.085 578.8 Example 43-A 110 Compound 43e-A 0.11 1000 Example 43-B 78.4 Compound 43e-B 0.035 2240 Example 44-A 65.4 Compound 43e-B 0.035 1868.6 Example 44-B 96.7 Compound 43e-A 0.11 879.1 nd 45e-B Example 45-A 153 or 0.26 or 0.39 588 or 392 Compound 45e-A Compound 45e-B Example 45-B >1000 or 0.26 or 0.39 >3846 or >2564 Compound 45e-A Compound 45e-A Example 46-A 45.5 or 0.26 or 0.39 175 or 116.7 Compound 45e-B Compound 45e-B Example 46-B 45.7 or 0.26 or 0.39 175.7 or 117.2 Compound 45e-A Compound 47e-A Example 47-A 10.9 or 0.021 or 0.025 519.0 or 436 Compound 47e-B nd 47e-A Example 47-B 13.1 0.021 or 0.025 623.8 or 524 Compound 47e-B Compound 47e-A e 48-A 18.3 0.021 or 0.025 871.4 or 732 Compound 47e-B Compound 47e-A Example 48-B 20.8 or 0.021 or 0.025 990.5 or 832 Compound 47e-B lism of prodrugs of compound of formula (I) A study was undertaken to evaluate the metabolic conversion of prodrugs, compound of formula (I), to its corresponding active form. The compounds of formula (I), if served as gs, can be metabolized to the active compound or other compounds of the invention in the body. Human liver microsomes are often used to assess the degree of lic conversion of prodrugs in the body of animal or human.

Materials NADPH cofactor system including β-Nicotinamide adenine dinucleotide phosphate (NADP), isocitric acid and isocitric dehydrogenase were purchased from Aldrich Co. (St.

Louis, MO, USA). Human liver microsomes (Cat No. 452117, Lot No. 38290) were obtained from Corning (Woburn, MA, USA). Mouse liver microsomes (Cat No. M1000, Lot No.1310028) were obtained from Xenotech.

Working on of the compounds and other solution Compounds were dissolved in DMSO to make 10 mM stock solutions. 10 µL of the stock solution was diluted with acetonitrile (990 µL) to get a 100 µM working solution.

Incubation Microsomes were preincubated with test compound for 10 min at 37°C in 100 mM ium phosphate buffer with pH 7.4. The reactions were initiated by adding NADPH regenerating system to give a final incubation volume of 200 μL and shaken in a water bath at 37°C. Incubation mixtures consisted of liver microsomes (0.5 mg microsomal protein/mL), substrates (1.0 μM), and NADP (1 mM), isocitric dehydrogenase(1 unit/mL), ric acid (6 Preparation of Samples for Analysis At 30 min, reaction was quenched by adding 600 μL cold acetonitrile (including 100 ng/mL tolbutamide and 100 ng/mL lol as internal rd). The s were centrifuged at 4000 rpm for 20 minutes and the resultant supernatants were subjected to MS analysis.

The samples for ation curve were prepared as followed. Dispense 100 μL/well liver microsomes and 98 μL/well NADPH rating system solution to 96-well plate. Add 600 μL ing solution first, and then followed by 2 µL Standard curve and QC working solution.

Bioanalysis The compounds were quantified on an API4000 LC-MC/MC instrument in the ESIPositive MRM mode.

A study was undertaken to evaluate the metabolic conversion of prodrugs (1µM), Example 1, Example 1-A, Example 1-B, Example 2, Example 2-A, Example 2-B, Example 3, Example 4, Example 5, Example 6, e 7, e 8, Example 9, Example 10, Example 11, Example 12, Example 13, Example 14, Example 15, Example 16, Example 17, Example 21, Example 22, Example 23, Example 25, Example 26, Example 27, e ple 29, Example 30, Example 31, Example 32, Example 33, Example 34-A, Example 34-B, Example 36-A, Example 36-B, Example 37-A, e 37-B, Example 38-A, Example 38-B, Example 39, Example 40, Example 41, Example 41-A, Example 41-B, Example 42, Example 42-A, Example 42-B, Example 43, Example 43-A, Example 43-B, Example 44, Example 44-A, Example 44-B and Example 45-A, Example 46-A, Example 46- B, Example 47-A, Example 47-B, Example 48-A, Example 48-B to the corresponding active forms, Compound 1e, Compound 1e-A, Compound 1e-B, Compound 34e-A, Compound 34e-B, Compound 36g-A, Compound 36g-B, nd 36g, Compound 41c, Compound 41c-B, Compound 41c-A, Compound 43e, Compound 43e-A, Compound 43e-B, Compound 45e-A, Compound 45e-B, Compound 47e-A, and Compound 47e-B in the presence of human liver microsomes. Results were summarized and shown in Table 2.

Table 2. Metabolic conversion of prodrugs in human liver microsomes lized Metabolized product product Corresponding Corresponding concentration tration Example No. Metabolized Product Example No. Metabolized Product in human liver in human liver (active form) (active form) microsomes microsomes (µM) (µM) Example 1 Compound 1e 0.0214 Example 31 Compound 1e 0.005 e 1-A Compound 1e-A 0.018 e 32 Compound 1e 0.013 Example 1-B Compound 1e-B 0.022 Example 33 Compound 1e 0.59 Example 2 Compound 1e 0.028 Example 34-A nd 34e-A 0.2 Example 2-A Compound 1e-B 0.036 e 34-B Compound 34e-B 0.088 Example 2-B Compound 1e-A 0.029 Example 36-A Compound 36g-A 0.02 Example 3 Compound 1e 0.12 Example 36-B Compound 36g-B 0.019 Example 5 Compound 1e 0.078 Example 37-A Compound 36g-A 0.004 Example 6 Compound 1e 0.074 Example 37-B Compound 36g-B 0.002 Example 7 Compound 1e 0.15 Example 38-A Compound 36g-A 0.026 Example 8 Compound 1e 0.043 Example 38-B nd 36g-B 0.034 Example 9 Compound 1e 0.002 Example 40 Compound 36g 0.032 Example 10 Compound 1e 0.005 Example 41-A Compound 41c-B 0.38 e 11 Compound 1e 0.001 e 41-B Compound 41c-A 0.36 Example 12 nd 1e 0.018 Example 42-A Compound 41c-A 0.14 Example 13 Compound 1e 0.04 Example 42-B Compound 41c-B 0.004 Example 14 Compound 1e 0.026 Example 43-A Compound 43e-A 0.014 Example 15 Compound 1e 0.002 Example 43-B Compound 43e-B 0.016 Example 16 Compound 1e 0.024 Example 44-A nd 43e-B 0.002 Example 17 Compound 1e 0.075 Example 44-B Compound 43e-A 0.002 Example 21 Compound 1e 0.48 Example 45-A Compound 45e-B 0.41 Compound 45e-A Example 22 Compound 1e 0.42 Example 46-A Compound 45e-A 0.039 Compound 45e-B Example 23 Compound 1e 0.42 Example 46-B Compound 45e-B 0.18 Compound 45e-A Example 25 Compound 1e 0.018 Example 47-A Compound 47e-A 0.36 Compound 47e-B Compound 47e-B Example 26 Compound 1e 0.042 Example 47-B or 0.41 nd 47e-A Example 27 Compound 1e 0.11 Example 48-A nd 47e-A 0.11 Compound 47e-B Example 28 Compound 1e 0.084 Example 48-B Compound 47e-B 0.053 Compound 47e-A Example 29 Compound 1e 0.009 Example 51 In vivo antiviral efficacy of e 43-A in AAV-HBV mouse model Animal model 4-6 week old male C57BL/6 mice, ic pathogen free, were purchased from Shanghai Laboratory Animal Center of Chinese Academy of Sciences (SLAC) and housed in an animal care facility in individually ventilated cages under controlled ature and light ions following the Institutional Animal Care guidelines. V virus was purchased from Beijing FivePlus Molecular Medicine Institute (Beijing, China). The recombinant virus carries 1.3 copies of the HBV genome packaged into AAV serotype 8 (AAV8) capsids. C57BL/6 mice were injected with 200µL of the recombinant virus diluted in saline buffer through tail vein. On day 14, the mice were bled to measure HBV surface antigen (HBsAg) and HBV genomic DNA in the serum, and animals were then randomized into groups according to these HBV biomarkers.

Measurement of HBV kers Serum HBsAg and HBeAg were measured using CLIA kits (Autobio Diagnostics Co., Ltd., Zhengzhou, China) according to the manufacturer’s instructions. The lower limit of detection for HBsAg was 0.05 IU/mL. Serum dilution of 500-fold was used to obtain values within the linear range of the standard curve.

Serum HBV DNA was extracted using a MagNA Pure 96 DNA and Viral NA Small Volume Kit (Roche) following the manufacturer’s instructions. The DNA samples were analyzed by real-time quantitative PCR (qPCR) using a HBV-specific primer and probe set for specific amplification and detection of a 128bp HBV genome region from the nucleotide 2969 to 3096. The sequences of the primers and probe are: Forward primer: AAGAAAAACCCCGCCTGTAA; Reverse primer: CCTGTTCTGACTACTGCCTCTCC; HBV-Probe: 5'TAMRA-CCTGATGTGATGTTCTCCATGTTCAGC-BHQ2-3'.

Anti-HBs in the serum was tested using Anti-HBs CLIA kits (Autobio stics Co., Ltd., hou, China) and mouse anti-IgG conjugated with Biotin (0.5 mg/mL) from a Mabtech B t kit. The gG Biotin was diluted in PBS with a final concentration of 1μg/mL. 25 μL of mouse anti-IgG were mixed with serum samples in wells of the plate in the Anti-HBs CLIA kit for 1-hour incubation. Then wash the plate and add Streptavidin-HRP for 1- hour incubation at room temperature. After repeating the washing step, mix substrate A and B from the CLIA kit and add 50 μL of the mixture in each well. After 5-min incubation at room temperature, the plate was read on an Envision Plate Reader (PerkinElmer) to measure luminecence.

Study design and results The mouse model with high level sion of both HBV DNA and HBsAg was generated by injecting C57BL/6 mice with a recombinant adeno-associated virus (AAV) carrying a replicable HBV genome (AAV-HBV). With long-lasting HBV viremia and fully competent immune system, the AAV-HBV mouse model was utilized to evaluate the antiviral efficacy of the TLR7 agonists following the study design as shown in Table 3.

Table 3. In vivo efficacy test of Example 43-A in AAV-HBV mouse model Animal group Test article Route Frequency ent (mg/kg) 1 Vehicle 0 PO QOD 42 days 2 10 PO QOD 42 days Example 43-A 3 10 PO QW 42 days Specifically, groups 2 and 3 were orally dosed with e 43-A at 10 mg/kg every other day (QOD) and once weekly (QW), respectively, and the control group 1 received only e. At the dosing volume of 10 mL/kg, Example 43-A (1 mg/mL) was formulated as an inclusion complex with 2% Klucel LF, 0.5% TPGS, 0.09% Methylparabens, 0.01% Propylparabens in water. The animals were treated for a total of 42 days, and were submandibularly bled twice per week for serum collection throughout the study. The serum samples were subjected to analysis of HBV biomarkers.

As shown in Figure 4, the treatment of e 43-A at 10 mg/kg QOD resulted in a dramatic reduction in HBV DNA (> 3 log) and HBsAg (> 2.8 log). At the end of the 42-day treatment, the levels of these viral markers became undetectable and below the lower limit of quantification (LLOQ). Even with the less frequent QW dosing, Example 43-A significantly reduced both HBV DNA (> 2 log) and HBsAg (>2.8 log). Moreover, the treatment of Example 43-A at 10 mg/kg, regardless of QOD and QW , induced a considerable level of anti- HBsAg antibody. In conclusion, Example 43-A demonstrated good in vivo anti-HBV activity by reducing HBV viral markers and promoting the production of HBV-specific antibody.

Example 52 In vivo ral cy of Example 41-A in AAV-HBV mouse model The antiviral efficacy of Example 41-A was evaluated in the same AAV-HBV model following the study design in Table 4 with the same methods to measure HBV biomarkers as described in Example 51.

Table 4 . In vivo efficacy test of Example 41-A in V mouse model Animal Dose Test article Route Frequency ent group (mg/kg) 1 Vehicle 0 PO QOD 42 days 2 1 PO QOD 42 days 3 3 PO QOD 42 days Example 41-A 4 10 PO QOD 42 days 10 PO QW 42 days Specifically, groups 2, 3 and 4 were orally dosed with Example 41-A at 1, 3 and 10 mg/kg QOD respectively. Group 5 was treated with 10 mg/kg QW, while group 1 with only Vehicle. At the dosing volume of 10 mL/kg, e 41-A (0.1, 0.3, and 1 mg/mL) was formulated as an inclusion complex with 2% Klucel LF, 0.5% TPGS, 0.09% Methylparabens, 0.01% Propylparabens in water. The animals were treated for a total of 42 days, and were submandibularly bled twice per week for serum collection throughout the study. The serum samples were subjected to is of HBV biomarkers.

As shown in Figure 5, the treatment of Example 41-A at 1, 3, 10 mg/kg QOD dose- ently reduced HBV DNA and HBsAg. All three doses d to reduce these viral markers below or close to the LLOQ at the end of the 42-day treatment. Even with the less frequent QW dosing, Example 41-A at 10 mg/kg also d HBV DNA and HBsAg to undetectable levels at the treatment end. Moreover, Example 41-A induced significantly higher levels of antibody against-HbsAg than Vehicle post treatment. In conclusion, Example 41-A demonstrated good in vivo anti-HBV activity by reducing HBV viral markers and promoting the production of HBV-specific antibody.

Example 53 In vivo antiviral of Example 42-A cy in AAV-HBV mouse model The antiviral cy of Example 42-A was evaluated in the same AAV-HBV model following the study design in Table 5 with the same methods to measure HBV biomarkers as described in Example 51.

Table 5. In vivo efficacy test of Example 42-A in AAV-HBV mouse model Animal Dose Test article Route Frequency Treatment group (mg/kg) 1 Vehicle 0 PO QOD 42 days 2 1 PO QOD 42 days Example 3 3 PO QOD 42 days 4 10 PO QOD 42 days ically, groups 2, 3, and 4 were orally dosed with Example 42-A at 1, 3, and 10 mg/kg QOD respectively, while group 1 with only Vehicle. At the dosing volume of 10mL/kg, Example 42-A (0.1, 0.3, and 1 mg/mL) was formulated as an inclusion complex with 2% Klucel LF, 0.5% TPGS, 0.09% Methylparabens, 0.01% Propylparabens in water. The animals were treated for a total of 42 days, and were submandibularly bled twice per week for serum collection throughout the study. The serum samples were subjected to analysis of HBV biomarkers.

As shown in Figure 6, the treatment of Example 42-A at 1, 3, 10 mg/kg QOD were all effective to reduce HBV DNA and HBsAg. While the higher doses led to faster clearance of HBV DNA and HBsAg, all three doses managed to reduce these viral markers below or close to the LLOQ at the end of the 42-day treatment. All the groups treated with Example 42-A ped significantly higher levels of anti-HBsAg dy. In conclusion, Example 42-A demonstrated good in vivo anti-HBV activity by reducing HBV viral markers and promoting the production of HBV-specific antibody.

Example 54 In vivo antiviral efficacy of Example 41-B in AAV-HBV mouse model The antiviral cy of Example 41-B was evaluated in the same AAV-HBV model following the study design in Table 6 with the same methods to measure HBV biomarkers as bed in Example 51.

Table 6. In vivo efficacy test of e 41-B in AAV-HBV mouse model Animal Dose Test article Route Frequency Treatment group (mg/kg) 1 Vehicle 0 PO QOD 42 days 2 1 PO QOD 42 days Example 3 3 PO QOD 42 days 4 10 PO QOD 42 days Specifically, groups 2, 3, and 4 were orally dosed with Example 41-B at 1, 3, and 10 mg/kg QOD, respectively, while group 1 with only Vehicle. At the dosing volume of 10 mL/kg, Example 41-B (0.1, 0.3, and 1 mg/mL) was formulated as an inclusion complex with 2% Klucel LF, 0.5% TPGS, 0.09% Methylparabens, 0.01% Propylparabens in water. The animals were treated for a total of 42 days, and were submandibularly bled twice per week for serum collection hout the study. The serum samples were ted to analysis of HBV biomarkers.

As shown in Figure 7, the treatment of Example 41-B at 1, 3, 10 mg/kg QOD were all ive to reduce HBV DNA and HBsAg. All three doses managed to reduce these viral markers below the LLOQ at the end of the 42-day treatment. All the groups treated with Example 41-B also developed high levels of anti-HBsAg antibody than the Vehicle group. In conclusion, Example 41-B demonstrated in vivo BV activity by reducing HBV viral markers and promoting the production of HBV-specific antibody.

Example 55 Single dose PK study in Male Wister-Han Rats The single dose PK in Male Wister-Han Rats was performed to assess pharmacokinetic properties of tested compounds. Two groups of animals were dosed via Gavage (POE) of the respective compound. Blood samples ximately 20 μL) were collected via Jugular vein or an ate site at 15 min, 30 min, 1H, 2 h, 4 h, 7 h and 24 h post-dose groups. Blood samples were placed into tubes containing EDTA-K2 agulant and centrifuged at 5000 rpm for 6 min at 4°C to separate plasma from the samples. After centrifugation, the resulting plasma was transferred to clean tubes for bioanalysis of both prodrug and active form on MS. In the groups that prodrug were dosed, the concentration of prodrugs in the plasma samples was under the detection limit. The “tested compound” in Table 8 was used as the internal standard for testing the metabolite (active form) of “dose compound” in vivo. The pharmacokinetic parameters were calculated using non-compartmental module of WinNonlin® Professional 6.2.

The peak concentration (Cmax) was recorded directly from mental observations. The area under the plasma concentration-time curve (AUC0-t) was calculated using the linear trapezoidal rule up to the last detectable concentration.

Cmax and AUC0-last are two critical PK parameters related to the in vivo efficacy of the tested nd. Compounds with higher Cmax and AUC0-last will lead to the better in vivo efficacy. Results of PK parameters following oral administration of active forms and competitor compounds are given in Table 7. The PK parameters of prodrugs are tabulated in Table 8. ing oral stration of prodrugs, the active forms were observed in plasma and ore tested. The exemplified prodrugs of present invention ( Example 41-B, 42-A, 42-B, 43-A, 45-A and 45-B) surprisingly showed much improved Cmax (5-175 folds increase) and AUC0-last (2.5-56 folds increase) comparing with reference compounds ( GS9620, S-2 and S-3) and compounds mentioned in present invention (Compound 41c-A, 41c-B and 43e-A) which are all active forms. The results clearly demonstrated the unexpected superiority of prodrugs over active forms on PK parameters which led to better in vivo efficacy.

Table 7. The mean plasma concentration and PK parameters of active forms after 5 mg/kg oral dosing Compound Dose compound GS9620 S-2 S-3 41c-A Time (h) Mean plasma tration(nM) 0.25 56.3 9.49 8.89 16.75 0.5 33.2 16.74 9.99 27.48 1 83.4 19.33 10.16 32.33 2 136 24.89 8.40 27.34 4 16.7 47.55 11.54 27.38 8* 9.49 52.72 8.17 18.02 24 ND 4.90 ND 5.60 Cmax (nM) 164 52.72 11.54 32.33 AUC0-last (nM⋅h) 316 748 95 242.5 nd Compound Compound Compound Dose compound 41c-B 43e-A 45e-A 45e-B Time (h) Mean plasma concentration(nM) 0.25 3.41 12.60 64.6 42.8 0.5 0.75 15.22 80.0 52.2 1 2.04 13.01 58.1 37.6 2 5.46 11.98 42.5 24.2 4 2.52 8.20 77.8 53.9 8* 1.21 6.31 34.6 29 24 ND ND 8.6 5.7 Cmax (nM) 5.46 15.22 80.0 53.9 AUC0-last (nM⋅h) 55.8 77 767 568 * 7 hrs for Compound 41c-A, Compound 41c-B and Compound 43e-A Table 8. PK parameters of prodrugs after 5 mg/kg oral dosing Dose compound Tested compound Cmax (nM) AUC0-last (nM⋅h) Example 41-B nd 41c-A 1315 3658 Example 42-A Compound 41c-A 1742 4867 e 42-B Compound 41c-B 956 3148 Example 43-A Compound 43e-A 77 229 Example 45-A Compound 45e-B 922 1914 Example 45-B Compound 45e-A 1436 2619 Example 56 LYSA solubility study LYSA study is used to determine the aqueous solubility of tested nds. Samples were prepared in duplicate from 10 mM DMSO stock solution. After evaporation of DMSO with a centrifugal vacuum evaporator, the compounds were ved in 0.05 M phosphate buffer (pH 6.5), stirred for one hour and shaken for two hours. After one night, the solutions were filtered using a iter filter plate. Then the te and its 1/10 dilution were analyzed by V.

In addition, a four-point calibration curve was prepared from the 10 mM stock solutions and used for the solubility determination of the compounds. The results were in µg/mL. In case the percentage of sample measured in on after evaporation divided by the calculated maximum of sample amount was bigger than 80%, the solubility was reported as bigger than this value.

Results of LYSA were shown in Table 9. It was clear that the solubility of active forms were surprisingly improved by 10 to over 200 folds when ted to various prodrugs.

Table 9. Solubility data of particular compounds LYSA of LYSA of Active Corresponding Active Prodrugs Prodrugs Forms Forms (µg/mL) (µg/mL) Example 1 290 Compound 1e 21 Example 1-A 315 Compound 1e-A 56 Example 1-B 200 nd 1e-B 50 Example 2 615 Compound 1e 21 Example 2-A >600 Compound 1e-B 50 Example 2-B >590 Compound 1e-A 56 Example 3 240 Compound 1e 21 Example 4 695 Compound 1e 21 Example 5 >595 Compound 1e 21 Example 6 140 Compound 1e 21 Example 7 615 Compound 1e 21 Example 8 620 Compound 1e 21 Example 9 >520 Compound 1e 21 Example 10 120 Compound 1e 21 Example 11 >618 Compound 1e 21 Example 12 120 Compound 1e 21 Example 13 155 Compound 1e 21 Example 14 225 Compound 1e 21 Example 15 405 Compound 1e 21 Example 16 205 Compound 1e 21 Example 17 190 Compound 1e 21 Example 25 >670 Compound 1e 21 e 26 >690 Compound 1e 21 Example 27 >380 nd 1e 21 Example 28 695 Compound 1e 21 Example 29 395 Compound 1e 21 Example 32 125 Compound 1e 21 Example 36-A 168 Compound 36g-A 6 Example 36-B 209 Compound 36g-B 11 Example 41-A 260 Compound 41c-B 5 Example 41-B 250 Compound 41c-A 1 Example 42-A 225 Compound 41c-A 1 Example 42-B 335 Compound 41c-B 5 Example 43-A 203 Compound 43e-A 13 Example 43-B 170 Compound 43e-B 13 Example 45 172 Compound 45e 152 Example 45-A >560 Compound 45e-A or 90 or 115 nd 45e-B Example 45-B 420 Compound 45e-B 115 or 90 Or Compound 45e-A Example 46-A 205 nd 45e-A 90 or 115 Or Compound 45e-B Example 46-B >580 Compound 45e-B 115 or 90 Or Compound 45e-A e 47-A 154 Compound 47e-A or <1.0 or <1.0 Compound 47e-B Example 47-B 128 Compound 47e-B or <1.0 or <1.0 Compound 47e-A Example 48-A 305 Compound 47e-A or <1.0 or <1.0 Compound 47e-B e 48-B 275 Compound 47e-B or <1.0 or <1.0 Compound 47e-A Example 57 Portal Vein Study The objective of this study was to understand whether g remains unchanged as it was ed through the intestine into the portal circulation and demonstrate the primary site of conversion.

Surgical procedure for Portal vein cannulation (PVC) and Carotid artery cannulation (CAC) Surgery was performed under pentobarbital /isoflurane anesthesia. y, after disinfecting the abdominal area with betadine and 70% isopropyl alcohol, a small abdominal mid-line incision was made. The cecum was pulled out and mesenteric vein was identified and isolated for about 5 mm . A loose ligature was placed proximally and distal end of the vein was ligated. Make a small incision (just enough to allow the insertion of the catheter) on isolated vein and insert the PU catheter towards liver for appropriate length. The catheter was secured in place by tying the loose ligature around the cannulated vessel. The cecum was replaced into abdominal cavity. A hole was made in the right abdominal wall to make the end of catheter pass . The catheter was secured by suture on the abdominal wall. The abdominal muscle incision was closed with suture. A small incision was made in the scapular area to serve as the exit site of the catheter. The er was subcutaneously tunneled and exteriorized through the scapular incision. A fixed suture was placed in the scapular region. The patency of the er was d and then exteriorized from the subcutaneous space to the dorsal neck region. After gently wiping the area, the abdominal cavity was sutured. The left carotid artery was then cannulated by inserting a PE50 er. Both the exteriorized catheters were tied firmly on the dorsal neck region and fixed. The animals was then allowed to recover in its cage and used for study at least 3 days after surgery. All catheters were flushed once daily with heparinized saline to maintain patency.

Oral PK study in PVC/CAC dual cannulated rat Animals were fasted overnight (n=3) and administered vial oral gavage kg, 10mL/kg). Blood samples (60 μL) were collected simultaneously from the portal and carotid artery catheters at 0.083, 0.25, 0.5, 1, 2, 4, 7, 24h. All blood samples will be transferred into entrifuge tubes containing 2 μL of K2EDTA (0.5M) as anti-coagulant and placed on wet ice. Then blood samples will be processed for plasma by centrifugation at approximately 4 °C, 3000g within half an hour of collection. Plasma samples will be stored in opylene tubes, quick frozen over dry ice and kept at -70±10oC until LC/MS/MS analysis. cokinetic parameters (mean ± SD, n= 3) of prodrugs and active forms in portal and carotid samples following oral administration of prodrugs (10 mg/kg) in portal vein cannulated rat were detected and analyzed. The test results of Example 1-B, 41-A, 41-B, 42-A and 43-A were summarized below.

Table 10. Pharmacokinetic parameters of Example 41-A and its corresponding active form nd 41c-B in portal and carotid samples following oral administration of Example 41-A (10 mg/kg) in portal vein cannulated rat Prodrug e 41-A Corresponding Active Compound 41c-B Portal sampling Carotid sampling PK parameter prodrug active form g active form Tmax (h) 0.14 0.4 0.19 0.42 Cmax (nM) 9703 2223 210 2185 AUC0-2 (nM⋅h) 2188 2246 114 2108 AUCactive/AUCtotal 51% 95% Table 11. Pharmacokinetic parameters of Example 43-A and its corresponding active form Compound 43e-A in portal and carotid samples following oral administration of Example 43-A (10 mg/kg) in portal vein cannulated rat Prodrug Example 43-A Corresponding Active Compound 43e-A Portal sampling Carotid sampling PK parameter prodrug active form prodrug active form Tmax (h) 0.28 0.33 0.22 0.28 Cmax (nM) 4110 818 191 691 AUC0-2 (nM⋅h) 2067 679 124 564 AUCactive/AUCtotal 25% 82% Table 12. Pharmacokinetic parameters of Example 1-B and its corresponding active form Compound 1e-A in portal and systemic samples following oral administration of Example 1-B (10 mg/kg) in portal vein cannulated rat Prodrug e 1-B Corresponding Active Compound 1e-A Portal sampling Carotid sampling PK parameter prodrug active form prodrug active form Tmax (h) 0.083 0.25 0.083 0.5 Cmax (nM) 670 192 70 174 AUC0-2 (nM⋅h) 266 164 40 184 AUCactive/AUCtotal 38% 82% Table 13. Pharmacokinetic parameters of Example 42-A and its ponding active form Compound 41c-A in portal and carotid s following oral administration of Example 42-A (10 mg/kg) in portal vein cannulated rat Prodrug Example 42-A Corresponding Active Compound 41c-A Portal sampling Carotid sampling PK parameter prodrug active form prodrug active form Tmax (h) 0.19 0.42 0.22 0.36 Cmax (nM) 8917 3162 286 3326 AUC0-2 (nM⋅h) 3461 3199 286 3326 AUCactive/AUCtotal 48% 96% Table 14. Pharmacokinetic parameters of Example 41-B and its corresponding active form nd 41c-A in portal and carotid samples following oral administration of Example 41-B (10 mg/kg) in portal vein cannulated rat Prodrug Example 41-B Corresponding Active Compound 41c-A Portal sampling d sampling PK parameter prodrug active form prodrug active form Tmax (h) 0.19 0.5 0.25 0.5 Cmax (nM) 7068 3315 29.6 3432 AUC0-2 (nM⋅h) 1444 3211 22.5 3301 AUCactive/AUCtotal 69% 99% Based on the above results, it was concluded that the primary site of conversion of prodrug was liver rather than intestine, because AUCactive/AUCtotal was higher in sampling from d artery compared to AUCactive/AUCtotal in sampling from portal vein.

Claims (9)

Claims

1. A compound of formula (I), wherein 5 R1 is C1-6alkyl; R2 is benzyl, said benzyl being unsubstituted or substituted by one, two or three substituents independently selected from halogen and C1-6alkyl; R3 is -NR4R5, wherein R4 is C1-6alkyl or C1-6alkoxyC1-6alkyl; 10 R5 is (C1-6alkyl)2NCOOC1-6alkyl, koxyC1-6alkyl, C1-6alkoxycarbonyl(C1- 6alkyl)aminoC1-6alkyl, C1-6alkoxycarbonyl(phenyl)C1-6alkyl, C1- 6alkoxycarbonylC1-6alkyl, C1-6alkoxycarbonyloxyC1-6alkyl, C1-6alkyl, C1- 6alkylcarbonyl(C1-6alkyl)aminoC1-6alkyl or pyrrolidinylcarbamoyloxyC1- 6alkyl; or 15 R4 and R5 together with the nitrogen they are attached to form a heterocyclyl; or pharmaceutically able salt, enantiomer or diastereomer thereof; with the proviso that 6-aminobenzyl(propylsulfonimidoyl)(pyrrolidinecarbonyl)purinone; 6-aminobenzyl(piperidinecarbonyl)(propylsulfonimidoyl)purinone; 20 6-aminobenzyl(morpholinecarbonyl)(propylsulfonimidoyl)purinone; obenzyl(3,3-dimethylpyrrolidinecarbonyl)(propylsulfonimidoyl)purinone; ethyl 1-[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]pyrrolidine carboxylate; 6-amino(2-azaspiro[3.3]heptanecarbonyl)benzyl(propylsulfonimidoyl)purinone; 25 6-aminobenzyl(2-oxaazaspiro[3.3]heptanecarbonyl)(propylsulfonimidoyl)purin obenzyl(3,3-difluoropyrrolidinecarbonyl)(propylsulfonimidoyl)purinone; 6-aminobenzyl(3-fluoromethyl-pyrrolidinecarbonyl)(propylsulfonimidoyl)purin- 8-one; and their enantiomers or diastereomers are excluded.

2. A compound according to claim 1, wherein R1 is C1-6alkyl; 5 R2 is benzyl, said benzyl being unsubstituted or substituted by n or kyl; R3 is azetidinyl; piperazinyl substituted by C1-6alkyl; piperidinyl substituted by piperidinyl; pyrrolidinyl; or 10 , wherein R4 is C1-6alkyl or C1-6alkoxyC1-6alkyl; R5 is (C1-6alkyl)2NCOOC1-6alkyl, C1-6alkoxyC1-6alkyl, C1-6alkoxycarbonyl(C1- 6alkyl)aminoC1-6alkyl, C1-6alkoxycarbonyl(phenyl)C1-6alkyl, C1- 6alkoxycarbonylC1-6alkyl, C1-6alkoxycarbonyloxyC1-6alkyl, C1-6alkyl, C1- 15 6alkylcarbonyl(C1-6alkyl)aminoC1-6alkyl or idinylcarbamoyloxyC1- 6alkyl.

3. A compound according to claim 1 or 2, wherein R1 is ethyl or propyl; 20 R2 is benzyl, bromobenzyl, chlorobenzyl, fluorobenzyl or methylbenzyl; R3 is azetidinyl;

4. -methylpiperazinyl; piperidinylpiperidinyl; idinyl; or 25 -NR4R5, wherein R4 is methyl, ethyl, propyl or methoxyethyl; R5 is (methyl)aminoethyl, butyl, butyl(methyl)carbamoyloxyethyl, diethylcarbamoyloxyethyl, ethoxycarbonyl(methyl)aminoethyl, ethoxycarbonylethyl, ethoxycarbonylisobutyl, ethoxycarbonylisopentyl, 30 ethoxycarbonylmethyl, ethoxycarbonyloxyethyl, ethoxycarbonyl(phenyl)ethyl, ethyl, isobutyl, isopropoxycarbonylisopentyl, isopropoxycarbonyl(phenyl)ethyl, isopropyl, methoxycarbonyl(methyl)aminoethyl, methoxyethyl, methoxypropyl, propyl, propyl(methyl)carbamoyloxyethyl, pyrrolidinylcarbamoyloxyethyl, tertbutoxycarbonyl (methyl)aminoethyl, tert-butoxycarbonylethyl, tertbutoxycarbonylisopentyl or tert-butoxycarbonyl(phenyl)ethyl. 5 4. A compound according to claim 3, wherein R3 is azetidinyl, 4-methylpiperazinyl, dinylpiperidinyl, pyrrolidinyl, acetyl(methyl)aminoethyl(methyl)amino, bis(methoxyethyl)amino, butyl(ethyl)amino, butyl(methyl)amino, butyl(methyl)carbamoyloxyethyl(methyl)amino, diethylcarbamoyloxyethyl(methyl)amino, ethoxycarbonyl(methyl)aminoethyl(methyl)amino, carbonylethyl(methyl)amino, 10 ethoxycarbonylisobutyl(methyl)amino, carbonylisopentyl(methyl)amino, ethoxycarbonylmethyl(methyl)amino, ethoxycarbonyloxyethyl(methyl)amino, ethoxycarbonyl(phenyl)ethyl(methyl)amino, ethyl(methyl)amino, isobutyl(methyl)amino, isopropoxycarbonylisopentyl(methyl)amino, isopropoxycarbonyl(phenyl)ethyl(methyl)amino, isopropyl(methyl)amino, methoxycarbonyl(methyl)aminoethyl(methyl)amino, 15 methoxyethyl(ethyl)amino, methoxyethyl(methyl)amino, methoxyethyl(propyl)amino, methoxypropyl(methyl)amino, propyl(ethyl)amino, propyl(methyl)amino, (methyl)carbamoyloxyethyl(methyl)amino, pyrrolidinylcarbamoyloxyethyl(methyl)amino, utoxycarbonyl(methyl)aminoethyl(methyl)amino, tert-butoxycarbonylethyl(methyl)amino, tert-butoxycarbonylisopentyl(methyl)amino or tert-butoxycarbonyl(phenyl)ethyl(methyl)amino. 5. A compound according to any one of claims 1 to 4, wherein R1 is ethyl. 6. A compound according to claim 1 or 2, wherein R2 is benzyl tuted by halogen or C1- 6alkyl. 7. A compound according to any one of claims 2 to 6, wherein R2 is enzyl, chlorobenzyl, fluorobenzyl or methylbenzyl. 8. A compound according to claim 7, wherein R2 is bromobenzyl, chlorobenzyl or fluorobenzyl. 9. A compound according to claim 1 or 2, wherein R3 is -NR4R5, wherein R4 is C1-6alkyl, R5 is C1-6alkyl. 10. A compound according to claim 9, n R3 is propyl(methyl)amino or ethyl(methyl)amino. 11. A compound according to any one of claims 1, 2, 6 and 9, wherein 5 R1 is C1-6alkyl; R2 is benzyl, said benzyl being substituted by halogen or C1-6alkyl; R3 is -NR4R5, wherein R4 is C1-6alkyl, R5 is C1-6alkyl. 12. A compound according to claim 11, wherein 10 R1 is ethyl; R2 is methylbenzyl, bromobenzyl, chlorobenzyl or fluorobenzyl; R3 is propyl(methyl)amino or ethyl(methyl)amino. 13. A compound selected from: 15 obenzyl-N-methyloxo-N-propyl(propylsulfonimidoyl)purinecarboxamide; 6-Aminobenzyl-N-(2-methoxyethyl)-N-methyloxo(propylsulfonimidoyl)purine carboxamide; 6-Aminobenzyl-N-ethyloxo-N-propyl(propylsulfonimidoyl)purinecarboxamide; 6-Aminobenzyl[4-(1-piperidyl)piperidinecarbonyl](propylsulfonimidoyl)purinone; 20 6-Aminobenzyl-N-ethyl-N-(2-methoxyethyl)oxo(propylsulfonimidoyl)purine amide; 6-Aminobenzyl-N-butyl-N-ethyloxo(propylsulfonimidoyl)purinecarboxamide; 6-Aminobenzyl-N-(2-methoxyethyl)oxo-N-propyl(propylsulfonimidoyl)purine carboxamide; 25 6-Aminobenzyl-N,N-bis(2-methoxyethyl)oxo(propylsulfonimidoyl)purine amide; 6-Amino(azetidinecarbonyl)benzyl(propylsulfonimidoyl)purinone; 6-Aminobenzyl-N-isopropyl-N-methyloxo(propylsulfonimidoyl)purinecarboxamide; 6-Aminobenzyl(4-methylpiperazinecarbonyl)(propylsulfonimidoyl)purinone; 30 6-Aminobenzyl-N-(3-methoxypropyl)-N-methyloxo(propylsulfonimidoyl)purine carboxamide; 6-Aminobenzyl-N-isobutyl-N-methyloxo(propylsulfonimidoyl)purinecarboxamide; Ethyl 2-[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino ]acetate; Ethyl 3-[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino ]propanoate; 5 tert-Butyl 3-[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl- amino]propanoate; Ethyl (2S)[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino ]propanoate; tert-Butyl (2S)[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl- 10 amino]methyl-pentanoate; Isopropyl (2S)[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino ]methyl-pentanoate; Ethyl (2S)[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino thyl-butanoate; 15 Ethyl (2S)[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino ]methyl-pentanoate; Ethyl (2S)[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino ]phenyl-propanoate; Isopropyl (2S)[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl3-phenyl-propanoate; tert-Butyl (2S)[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl- amino]phenyl-propanoate; N-[2-[Acetyl(methyl)amino]ethyl]aminobenzyl-N-methyloxo (propylsulfonimidoyl)purinecarboxamide; 25 Methyl N-[2-[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methylamino ]ethyl]-N-methyl-carbamate; utyl N-[2-[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl- amino]ethyl]-N-methyl-carbamate; Ethyl N-[2-[[6-aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl- 30 amino]ethyl]-N-methyl-carbamate; 2-[[6-Aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl-amino]ethyl N- butyl-N-methyl-carbamate; Aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl-amino]ethyl pyrrolidinecarboxylate; 2-[[6-Aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl-amino]ethyl N- methyl-N-propyl-carbamate; 5 2-[[6-Aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl-amino]ethyl N,N-diethylcarbamate; 2-[[6-Aminobenzyloxo(propylsulfonimidoyl)purinecarbonyl]-methyl-amino]ethyl ethyl carbonate; 6-Amino-N-butyl[(4-chlorophenyl)methyl]-N-methyloxo[S(S)- 10 propylsulfonimidoyl]purinecarboxamide; 6-amino-N-butyl[(4-chlorophenyl)methyl]-N-methyloxo[S(S)- propylsulfonimidoyl]purinecarboxamide; 6-Amino[(4-chlorophenyl)methyl]-N-ethyl-N-methyloxo(propylsulfonimidoyl)purine carboxamide; 15 6-Amino-N-methyloxo-N-propyl-2[S(S)-propylsulfonimidoyl](p-tolylmethyl)purine carboxamide; 6-Amino-N-methyloxo-N-propyl-2[S(R)-propylsulfonimidoyl](p-tolylmethyl)purine carboxamide; 6-Amino[S(S)-propylsulfonimidoyl](p-tolylmethyl)(pyrrolidinecarbonyl)purinone; 20 6-Amino[S(R)-propylsulfonimidoyl](p-tolylmethyl)(pyrrolidinecarbonyl)purinone; 6-Amino-N-(2-methoxyethyl)-N-methyloxo[S(S)-propylsulfonimidoyl](ptolylmethyl )purinecarboxamide; 6-Amino-N-(2-methoxyethyl)-N-methyloxo[S(R)-propylsulfonimidoyl](ptolylmethyl )purinecarboxamide; 25 6-Amino-N-ethyl-N-methyloxo(propylsulfonimidoyl)(p-tolylmethyl)purine amide; 6-Amino-N-butyl-N-methyloxo(propylsulfonimidoyl)(p-tolylmethyl)purine carboxamide; 6-Amino[(4-chlorophenyl)methyl][S(R)-ethylsulfonimidoyl]-N-methyloxo-N-propyl- 30 purinecarboxamide; 6-Amino[(4-chlorophenyl)methyl][S(S)-ethylsulfonimidoyl]-N-methyloxo-N-propylpurinecarboxamide 6-Amino[(4-chlorophenyl)methyl]-N-ethyl-2[S(S)-ethylsulfonimidoyl]-N-methyloxopurinecarboxamide 6-Amino[(4-chlorophenyl)methyl]-N-ethyl[S(R)-ethylsulfonimidoyl]-N-methyloxopurinecarboxamide 5 6-Amino[S(S)-ethylsulfonimidoyl]-N-methyloxo-N-propyl(p-tolylmethyl)purine carboxamide; 6-Amino[S(R)-ethylsulfonimidoyl]-N-methyloxo-N-propyl(p-tolylmethyl)purine carboxamide; 6-Amino-N-ethyl-2[S(S)-ethylsulfonimidoyl]-N-methyloxo(p-tolylmethyl)purine 10 carboxamide; 6-Amino-N-ethyl[S(R)-ethylsulfonimidoyl]-N-methyloxo(p-tolylmethyl)purine carboxamide; 6-Amino[S(S)ethylsulfonimidoyl][(4-fluorophenyl)methyl]-N-methyloxo-N-propylpurinecarboxamide 15 6-Amino[S(R)ethylsulfonimidoyl][(4-fluorophenyl)methyl]-N-methyloxo-N-propylpurinecarboxamide 6-Amino-N-ethyl(ethylsulfonimidoyl)[(4-fluorophenyl)methyl]-N-methyloxo-purine amide; 6-Amino-N-ethyl[S(S)-(ethylsulfonimidoyl)][(4-fluorophenyl)methyl]-N-methyloxo- 20 purinecarboxamide; 6-Amino-N-ethyl[S(R)-(ethylsulfonimidoyl)][(4-fluorophenyl)methyl]-N-methyloxopurinecarboxamide 6-Amino[(4-bromophenyl)methyl](ethylsulfonimidoyl)-N-methyloxo-N-propyl-purine- 7-carboxamide; 25 6-Amino[S(R)-ethylsulfonimidoyl][(4-bromophenyl)methyl]-N-methyloxo-N-propylpurinecarboxamide 6-Amino[S(S)-ethylsulfonimidoyl][(4-bromophenyl)methyl]-N-methyloxo-N-propylpurinecarboxamide o[(4-bromophenyl)methyl]-N-ethyl(ethylsulfonimidoyl)-N-methyloxo-purine 30 carboxamide; 6-Amino[(4-bromophenyl)methyl]-N-ethyl[S(S)-(ethylsulfonimidoyl)]-N-methyloxopurinecarboxamide ; and 6-Amino[(4-bromophenyl)methyl]-N-ethyl[S(R)-(ethylsulfonimidoyl)]-N-methyloxopurinecarboxamide or pharmaceutically acceptable salt, enantiomer or diastereomer thereof.

5. 14. A compound according to claim 13, selected from: 6-Aminobenzyl-N-methyloxo-N-propyl(propylsulfonimidoyl)purinecarboxamide; 6-Amino[(4-chlorophenyl)methyl][S(R)-ethylsulfonimidoyl]-N-methyloxo-N-propylpurinecarboxamide 6-Amino[(4-chlorophenyl)methyl][S(S)-ethylsulfonimidoyl]-N-methyloxo-N-propyl- 10 purinecarboxamide; 6-Amino[(4-chlorophenyl)methyl]-N-ethyl-2[S(S)-ethylsulfonimidoyl]-N-methyloxopurinecarboxamide o[(4-chlorophenyl)methyl]-N-ethyl[S(R)-ethylsulfonimidoyl]-N-methyloxopurinecarboxamide 15 6-Amino[S(S)-ethylsulfonimidoyl]-N-methyloxo-N-propyl(p-tolylmethyl)purine amide; 6-Amino[S(R)-ethylsulfonimidoyl]-N-methyloxo-N-propyl(p-tolylmethyl)purine carboxamide; 6-Amino-N-ethyl-2[S(S)-ethylsulfonimidoyl]-N-methyloxo(p-tolylmethyl)purine 20 carboxamide; 6-Amino-N-ethyl[S(R)-ethylsulfonimidoyl]-N-methyloxo(p-tolylmethyl)purine carboxamide; 6-amino(ethylsulfonimidoyl)[(4-fluorophenyl)methyl]-N-methyloxo-N-propyl-purine carboxamide; 25 6-Amino[S(S)ethylsulfonimidoyl][(4-fluorophenyl)methyl]-N-methyloxo-N-propylpurinecarboxamide ; and

6. -Amino[S(R)ethylsulfonimidoyl][(4-fluorophenyl)methyl]-N-methyloxo-N-propylpurinecarboxamide or pharmaceutically acceptable salt, enantiomer or diastereomer f. 15. A process for the preparation of a compound according to any one of claims 1 to 14 sing the following step: the reaction of a compound of formula (II), NH O O N N 1 R R (II), with carbamoyl chloride in the presence of a mixed base; wherein the mixed base is pyridine and triethylamine, ne and DIPEA, DMAP and triethylamine, or DMAP and DIPEA; R1 and R2 are defined as in any one of claims 1 to 14. 16. A compound or pharmaceutically acceptable salt, enantiomer or diastereomer according to any one of claims 1 to 14 for use as therapeutically active substance. 1

7. A pharmaceutical composition comprising a compound in accordance with any one of claims 10 1 to 14 and a therapeutically inert carrier. 1

8. The use of a compound according to any one of claims 1 to 14 for the treatment or prophylaxis of hepatitis B virus infection. 15 1

9. The use of a compound according to any one of claims 1 to 14 for the ation of a medicament for the treatment or prophylaxis of hepatitis B virus infection. 20. The use of a compound according to any one of claims 1 to 14 as the TLR7 t. 20 21. The use of a compound according to any one of claims 1 to 14 to induce tion of interferon-α. 22. A compound or pharmaceutically acceptable salt, enantiomer or diastereomer according to any one of claims 1 to 14 for the treatment or prophylaxis of hepatitis B virus infection. 23. A nd or pharmaceutically able salt, enantiomer or diastereomer according to any one of claims 1 to 14, when manufactured according to a process of claim 15. 23. A method for the treatment or prophylaxis of hepatitis B virus infection, which method comprises administering a therapeutically ive amount of a compound as defined in any one of claims 1 to 14. 24. The invention as hereinbefore described. WO 41763 W0 4]763 WO 41763 6 HBsAg g 5 -o- Vehicle 8 + 43-A10mg/kg QOD E 4 + 43—A 10mg/kg QW 2 10 1.4 LLOQ 0 7 14 21 28 35 42 Days post first administration * values below LLOQ HBV DNA + Vehicle 2 4