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FR2100698A1 - 4-amino-1-substd-1h-pyrazolo (3,4-b) pyridine -5-carboxylic acids - and esters cns depressants antiinflammatories - Google Patents

4-amino-1-substd-1h-pyrazolo (3,4-b) pyridine -5-carboxylic acids - and esters cns depressants antiinflammatories

Info

Publication number
FR2100698A1
FR2100698A1 FR7119340A FR7119340A FR2100698A1 FR 2100698 A1 FR2100698 A1 FR 2100698A1 FR 7119340 A FR7119340 A FR 7119340A FR 7119340 A FR7119340 A FR 7119340A FR 2100698 A1 FR2100698 A1 FR 2100698A1
Authority
FR
France
Prior art keywords
alkyl
antiinflammatories
substd
pyrazolo
pyridine
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
FR7119340A
Other languages
French (fr)
Other versions
FR2100698B1 (en
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
ER Squibb and Sons LLC
Original Assignee
ER Squibb and Sons LLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by ER Squibb and Sons LLC filed Critical ER Squibb and Sons LLC
Publication of FR2100698A1 publication Critical patent/FR2100698A1/en
Application granted granted Critical
Publication of FR2100698B1 publication Critical patent/FR2100698B1/fr
Granted legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic 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
    • C07D231/14Heterocyclic 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 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
    • C07D231/38Nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

The new cpds are of formula: in which R is H or alkyl, R1 is alkyl, phenyl or phenyl alkylene, R2 is H or alkyl, R3 and R4 are H, alkyl, phenylalkylene, dialkylamino-alkylene or R5, R6-phenyl where R5 and R6 are H, alkyl, CF3 or COOH, or NR3R4 represents R7, R8-pyrrolidino, R7, R8 pyridazinyl R7, R8-piperidino, R7, R8-pyrazolyl, R7, R8-pyrimidyl R7, R8 dihydropyridazinyl or R7, R8-piperazinyl, where R7 and R8 are H, alkyl or hydeozyalkyl, (all alkyl gps being lower alkyl) together with their acid addn salts. They are prepared by reaction of the corres. 4-alkoxy, or 4-halo-cpds with HNR3R4. They have CNS depressant antiinflammatory and analgesic activity, and may be used in the treatment of asthma.
FR7119340A 1970-05-28 1971-05-27 4-amino-1-substd-1h-pyrazolo (3,4-b) pyridine -5-carboxylic acids - and esters cns depressants antiinflammatories Granted FR2100698A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US4156870A 1970-05-28 1970-05-28

Publications (2)

Publication Number Publication Date
FR2100698A1 true FR2100698A1 (en) 1972-03-24
FR2100698B1 FR2100698B1 (en) 1974-08-23

Family

ID=21917210

Family Applications (1)

Application Number Title Priority Date Filing Date
FR7119340A Granted FR2100698A1 (en) 1970-05-28 1971-05-27 4-amino-1-substd-1h-pyrazolo (3,4-b) pyridine -5-carboxylic acids - and esters cns depressants antiinflammatories

Country Status (13)

Country Link
JP (1) JPS554105B1 (en)
BE (1) BE767842A (en)
CA (1) CA920592A (en)
CH (1) CH527208A (en)
DE (1) DE2123318C2 (en)
ES (1) ES390163A1 (en)
FR (1) FR2100698A1 (en)
HU (1) HU163173B (en)
IE (1) IE35118B1 (en)
NL (1) NL172657C (en)
SE (1) SE367202B (en)
YU (1) YU37344B (en)
ZA (1) ZA711710B (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2187781A1 (en) * 1972-06-13 1974-01-18 Fratmann Ag
FR2189037A1 (en) * 1972-06-16 1974-01-25 Squibb & Sons Inc
FR2206102A1 (en) * 1972-11-15 1974-06-07 Squibb & Sons Inc

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3804843A (en) * 1971-12-23 1974-04-16 Squibb & Sons Inc Amino derivatives of pyrazolopyridine carbonitriles
US3833598A (en) * 1972-12-29 1974-09-03 Squibb & Sons Inc Amino derivatives of pyrazolopyridine-6-carboxylic acids and esters
EP2690101B1 (en) 2007-12-19 2015-06-24 Genentech, Inc. 5-Anilinoimidazopyridines and Methods of Use
PE20110570A1 (en) * 2008-07-01 2011-08-26 Genentech Inc REPLACED BICYCLE HETEROCYCLES
CA2727252A1 (en) 2008-07-01 2010-01-07 Genentech, Inc. Isoindolone derivatives as mek kinase inhibitors and methods of use

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2187781A1 (en) * 1972-06-13 1974-01-18 Fratmann Ag
FR2189037A1 (en) * 1972-06-16 1974-01-25 Squibb & Sons Inc
FR2206102A1 (en) * 1972-11-15 1974-06-07 Squibb & Sons Inc

Also Published As

Publication number Publication date
DE2123318C2 (en) 1984-05-03
ES390163A1 (en) 1973-07-01
SE367202B (en) 1974-05-20
CA920592A (en) 1973-02-06
CH527208A (en) 1972-08-31
FR2100698B1 (en) 1974-08-23
NL172657B (en) 1983-05-02
HU163173B (en) 1973-06-28
IE35118L (en) 1971-11-28
NL7106688A (en) 1971-11-30
DE2123318A1 (en) 1971-12-09
JPS554105B1 (en) 1980-01-29
NL172657C (en) 1983-10-03
BE767842A (en) 1971-11-29
YU106671A (en) 1983-04-27
ZA711710B (en) 1971-12-29
IE35118B1 (en) 1975-11-12
YU37344B (en) 1984-08-31

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