GB1134852A - Biologically active pyrazolopyrimidines - Google Patents
Biologically active pyrazolopyrimidinesInfo
- Publication number
- GB1134852A GB1134852A GB2139665A GB2139665A GB1134852A GB 1134852 A GB1134852 A GB 1134852A GB 2139665 A GB2139665 A GB 2139665A GB 2139665 A GB2139665 A GB 2139665A GB 1134852 A GB1134852 A GB 1134852A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- reacting
- formula
- alkyl group
- substituted
- 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.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
1,134,852. Substituted pyrazolo-pyrimidines. WELLCOME FOUNDATION Ltd. (Burroughs Wellcome & Co. (U.S.A.)). 19 May, 1966 [20 May, 1965], No. 21396/65. Heading C2C. Novel compounds of the Formula (I) or tautomers thereof, in which X is a hydrogen atom or a hydroxy group. R<SP>1</SP> is an alkyl group of 1 to 3 carbon atoms when X is hydrogen, and an alkyl group of 2 or 3 carbon atoms when X is hydroxy are prepared by: (a) reacting a 3-amino-4- alkylcarboxamidopyrazole with a compound H.CO.Z where the alkyl group is R<SP>1</SP> and Z is a substituted or unsubstituted amino, alkoxy or hydroxy group, and cyclizing, if necessary, with heat; or (b) reacting the same 3-amino-4- alkylcarboxamidopyrazole with a compound A.CO.B wherein A and B are the same or different and may be amino or alkoxy groups, or halogen atoms, or taken together, an imino group, and heating if necessary; or (c) reacting a 3 - amino - 4 - carbalkoxypyrazole with R<SP>1</SP>NCO and cyclizing with ethanol and HC1. Specified compounds of Formula (I) are 4- oxo - 5 - N - methyl - 4,5 - dihydropyrazolo- (3,4-d) pyrimidine, and the 5-N-ethyl and 5-N- n-propyl analogues, and 4,6-dioxo-5-N-ethyl- 4,5,6,7 - tetrahydropyrazolo - (3,4 - d) - pyrimidine and the 5-N-n-propyl analogue. 3 - Amino - 4 - N - methylcarboxamidopyrazole is prepared by treating 3-amino-4-carbethoxypyrazole with methylamine in the presence of sodium methoxide. Pharmaceutical compositions for the inhibition of xanthrine oxidase, for treatment of hyperuricemias and as potentiators for antimetabolic 6-substituted purines comprise compounds of the Formula (I) in admixture with carriers in the form of tablets, capsules, cachets, ampoules, suppositories, powders, granules, ointments and aqueous, non-aqueous or emulsified liquids.
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2139665A GB1134852A (en) | 1965-05-20 | 1965-05-20 | Biologically active pyrazolopyrimidines |
CH728666A CH484929A (en) | 1965-05-20 | 1966-05-18 | Process for the preparation of pyrazolo (3,4-d) pyrimidines |
ES0326892A ES326892A1 (en) | 1965-05-20 | 1966-05-18 | A method for the production of a xantin oxidase inhibitor. (Machine-translation by Google Translate, not legally binding) |
BE681349D BE681349A (en) | 1965-05-20 | 1966-05-20 | |
FR62302A FR1480652A (en) | 1965-05-20 | 1966-05-20 | Pyrimidine derivatives and their preparation |
FR73604A FR5679M (en) | 1965-05-20 | 1966-08-19 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2139665A GB1134852A (en) | 1965-05-20 | 1965-05-20 | Biologically active pyrazolopyrimidines |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1134852A true GB1134852A (en) | 1968-11-27 |
Family
ID=10162223
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2139665A Expired GB1134852A (en) | 1965-05-20 | 1965-05-20 | Biologically active pyrazolopyrimidines |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE681349A (en) |
CH (1) | CH484929A (en) |
ES (1) | ES326892A1 (en) |
FR (1) | FR5679M (en) |
GB (1) | GB1134852A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6191136B1 (en) | 1997-11-07 | 2001-02-20 | Johns Hopkins University | Methods for treatment of disorders of cardiac contractility |
-
1965
- 1965-05-20 GB GB2139665A patent/GB1134852A/en not_active Expired
-
1966
- 1966-05-18 CH CH728666A patent/CH484929A/en not_active IP Right Cessation
- 1966-05-18 ES ES0326892A patent/ES326892A1/en not_active Expired
- 1966-05-20 BE BE681349D patent/BE681349A/xx unknown
- 1966-08-19 FR FR73604A patent/FR5679M/fr not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6191136B1 (en) | 1997-11-07 | 2001-02-20 | Johns Hopkins University | Methods for treatment of disorders of cardiac contractility |
US6569862B1 (en) | 1997-11-07 | 2003-05-27 | Johns Hopkins University | Methods for treatment of disorders of cardiac contractility |
Also Published As
Publication number | Publication date |
---|---|
FR5679M (en) | 1968-01-08 |
CH484929A (en) | 1970-01-31 |
ES326892A1 (en) | 1967-07-01 |
BE681349A (en) | 1966-11-21 |
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