ME02295B - Inhibitori neprilizina - Google Patents
Inhibitori neprilizinaInfo
- Publication number
- ME02295B ME02295B MEP-2015-180A MEP18015A ME02295B ME 02295 B ME02295 B ME 02295B ME P18015 A MEP18015 A ME P18015A ME 02295 B ME02295 B ME 02295B
- Authority
- ME
- Montenegro
- Prior art keywords
- 6alkyl
- 6alkylene
- phenyl
- alkyl
- halo
- Prior art date
Links
- 239000002792 enkephalinase inhibitor Substances 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 claims 8
- 125000005843 halogen group Chemical group 0.000 claims 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 7
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 5
- -1 -OH Chemical group 0.000 claims 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 4
- 125000003118 aryl group Chemical group 0.000 claims 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 3
- 229910052799 carbon Inorganic materials 0.000 claims 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 2
- 125000004076 pyridyl group Chemical group 0.000 claims 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 235000010290 biphenyl Nutrition 0.000 claims 1
- 239000004305 biphenyl Substances 0.000 claims 1
- 150000001721 carbon Chemical group 0.000 claims 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 1
- JFSPBVWPKOEZCB-UHFFFAOYSA-N fenfuram Chemical group O1C=CC(C(=O)NC=2C=CC=CC=2)=C1C JFSPBVWPKOEZCB-UHFFFAOYSA-N 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 claims 1
- 125000001624 naphthyl group Chemical group 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 125000004430 oxygen atom Chemical group O* 0.000 claims 1
- 125000003373 pyrazinyl group Chemical group 0.000 claims 1
- 125000003226 pyrazolyl group Chemical group 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 229920006395 saturated elastomer Polymers 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/08—Bridged systems
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- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
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- A61K31/341—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide not condensed with another ring, e.g. ranitidine, furosemide, bufetolol, muscarine
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- A61K31/415—1,2-Diazoles
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- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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- A61K31/445—Non condensed piperidines, e.g. piperocaine
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Claims (1)
1. Jedinjenje formule 1: gde:R1 je izabran između -OR7 i -NR8R9;R2 je H ili -P(O)(OH)2 ili je R2 uzet zajedno sa R7 da bi formirali -CR18R19 - ili je uzet zajedno sa R8 da bi formirali -C(O)-;X je –C1-9gheteroaril;R3 nije prisutan ili je izabran između H; halo; -C0-5alkilen-OH; -NH2 ; -C1-6alkila; -CF3; -C3-7cikloalkila; -C0-2alkilen-O-C1-6alkila; -C(O)R20; -C0-1alkilen-COOR21; -C(O)NR22R23; -NHC(O)R24; =O; -NO2; -C(CH3)=N(OH); fenila opciono supstituisanog sa jednom ili dvegrupe nezavisno izabrane između halo, -OH, -CF3, -OCH3, -NHC(O)CH3, i fenila;naftalenila; piridinila; pirazinila; pirazolila opciono supstituisanog sa metilom; tiofenilaopciono supstituisanog sa metilom ili halo; furanila; i -CH2-morfolinila; i R3, kada je prisutan, je povezan sa atomom ugljenika;R4 nije prisutan ili je izabran između sledećih : H; -OH; -C1-6alkila; -C1-2alkilen-COOR35; -CH2OC(O)CH(R36)NH2; -OCH2OC(O)CH(R36)NH2; -OCH2OC(O)CH3; -CH2OP(O)(OH)2 -CH2CH(OH)CH2OH; -CH[CH(CH3)2]-NHC(O)O-C1 -6alkila; piridinila; i fenila ili benzilaopciono supstituisanih sa jednom ili više grupa izabranih između halo, -COOR35, -OCH3, -OCF3, i -SCF3; i R4, kada je prisutan, povezan je sa atomom ugljenika ili azota;ili su R3 i R4 uzeti zajedno da bi formirali -fenilen-O-(CH2)1-3- ili -fenilen-O-CH2-CHOH-CH2-:a je 0 ili 1; R5 je izabran između halo, -CH3, -CF3, i -CN;b je 0 ili celi broj između 1 i 3; svaki R6 je nezavisno izabran između halo, -OH, -CH3, -OCH3, i -CF3;R7 je izabran između H, -C1-8alkila, -C1-3alkilen-C6-10arila, -C1-3alkilen-C1-9heteroarila, -C3-7cikloalkila, -[(CH2)2O]1-3CH3, -C1-6alkilen-OC(O)R10, -C1-6alkilen-NR12 R13, -C1 -6alkilenC(O)R31, -C0-6alkilenmorfolinila, -C1-6alkilen-SO2-C1-6alkila, R10 je izabran između -C1-6alkila, -O-C1-6alkila, -C3-7cikloalkila, -O-C3-7cikloalkila, fenila, -O-fenila, -NR12 R13, -CH[CH(CH3)2]-NH2, -CH[CH(CH3)2]-NHC(O)O-C1-6alkila, i-CH(NH2)CH2COOCH3; i R12 i R13 su nezavisno izabrani i zmeđu H, -C1-6alkila, i benzila; ilisu R12 i R13 uzeti zajedno kao -(CH2)3-6-, -C(O)-(CH2)3-, ili -(CH2)2O(CH2)2-; R31 je izabranizmeđu -O-C1-6alkila, -O-benzila, i -NR12 R13; i R32 je -C1-6alkil ili -C0-6alkilen-C6-10aril;R8 je izabran između H, -OH, -OC(O)R14, -CH2COOH, -O-benzila, -piridila, i -OC(S)NR15R16; R14 je izabran između H, -C1-6alkila, -C6-10arila, -OCH2-C6-10arila, -CH2O-C6-10arila, i -NR15R16; i R15 i R16 su nezavisno izabrani između H i -C1-4alkila;R9 je izabran između H, -C1-6alkila, i -C(O)-R17; i R17 je izabran između H, - C1-6alkila, -C3-7cikloalkila, -C6-10arila, i -C1-9heteroarila;R18 i R19 su nezavisno izabrani između H, -C1-6alkila, i -O-C3-7cikloalkila, ili su R18 i R19 uzetizajedno da bi formirali =O;R20 je izabran između H i -C1-6alkila;R21 i R35 su nezavisno izabrani i zmeđu H, -C1-6alkila, -C1-3alkilen-C6-10arila, -C1-3alkilen-C1-9heteroarila, -C3-7cikloalkila, -[(CH2)2O] 1-3CH3, -C1-6alkilen-OC(O)R25, -C1-6alkilen NR27R28, -C1-6alkilen-C(O)R33, -C0-6alkilenmorfolinila, -C1-6alkilen-SO2-C1-6alkila, R25 je izabran između -C1-6alkila, -O-C1-6alkila, -C3-7cikloalkila, -O-C3-7cikloalkila, fenila, -O-fenila, -NR27R28, -CH[CH(CH3)2]-NH2, -CH[CH(CH3)2]-NHC(O)O-C1-6alkila,CH(NH2)CH2COOCH3; R27 i R28 su nezavisno izabrani između H, -C1-6alkila, i benzila; ili suR27 i R28 uzeti zajedno kao -(CH2) 3-6-, -C(O)-(CH2)3-, ili -(CH2)2O (CH2)2 -; R33 je izabranizmeđu -O-C1-6alkila, -O-benzila, i -NR27R28; i R34 je -C1-6alkil ili -C0-6alkilen-C6-10aril;R22 i R23 su nezavisno izabrani između H, -C1-6alkila, -CH2COOH, -(CH2)2OH, -(CH2)2O CH3,-(CH2)2SO2NH2, -(CH2)2N(CH3)2, -C0-1alkilen-C1-7cikloalkila, i -(CH2)2-imidazolila; ili su R22 i R23 uzeti zajedno da bi formirali zasićeni ili delimično nezasićen i -C3-5heterocikl opciono supstituisan sa halo, -OH, -COOH, ili -CONH2; i opciono sadrže atom kiseonika u prstenu;R24 je izabran između -C1-6alkila; -C0-1alkilen-O-C1-6alkila; fenila opciono supstituisanog sahalo ili -OCH3; i -C1-9heteroarila; iR36 je izabran između H, -CH(CH3)2, fenila, i benzila;gde je svaka alkil grupa u R1 R3, i R4 opciono supstituisana sa 1 do 8 atoma fluora; i;gde je metilen linker na bifenilu opciono supstituisan sa jednom ili dve -C1-6alkil grupe ili ciklopropilom; ili sa njegovom farmaceutski prihvatljivom soli.
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| US8449890B2 (en) * | 2011-02-17 | 2013-05-28 | Theravance, Inc. | Neprilysin inhibitors |
| EP2714660B1 (en) | 2011-05-31 | 2018-09-26 | Theravance Biopharma R&D IP, LLC | Neprilysin inhibitors |
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| CN104470521B (zh) | 2012-06-08 | 2017-04-12 | 施万生物制药研发Ip有限责任公司 | 脑啡肽酶抑制剂 |
| PT2864292T (pt) | 2012-06-08 | 2017-07-10 | Theravance Biopharma R&D Ip Llc | Inibidores de neprisilina |
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| US8796305B2 (en) * | 2012-11-05 | 2014-08-05 | Bayer Pharma Aktiengesellschaft | Carboxy-substituted imidazo[1,2-a]pyridinecarboxamides and their use |
| EP2956445A1 (en) | 2013-02-14 | 2015-12-23 | Novartis AG | Substituted bisphenyl butanoic acid derivatives as nep inhibitors with improved in vivo efficacy |
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| CN115925679A (zh) | 2014-12-24 | 2023-04-07 | 株式会社Lg化学 | 作为gpr120激动剂的联芳基衍生物 |
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| CN112592294B (zh) * | 2020-12-22 | 2022-05-13 | 江苏阿尔法药业股份有限公司 | 一种沙库巴曲药物中间体的合成方法 |
| TW202333563A (zh) | 2021-11-12 | 2023-09-01 | 瑞士商諾華公司 | 用於治療疾病或障礙之二胺基環戊基吡啶衍生物 |
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