GB1295228A - - Google Patents

Info

Publication number
GB1295228A
GB1295228A GB1295228DA GB1295228A GB 1295228 A GB1295228 A GB 1295228A GB 1295228D A GB1295228D A GB 1295228DA GB 1295228 A GB1295228 A GB 1295228A
Authority
GB
United Kingdom
Prior art keywords
formula
acid addition
radical
july
reacting
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
Application number
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 filed Critical
Publication of GB1295228A publication Critical patent/GB1295228A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
    • C07H19/04Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/16Purine radicals

Abstract

1295228 Adenosine derivatives BOEHRINGER MANNHEIM GmbH 8 July 1971 [14 July 1970] 32182/71 Heading C2C Novel compounds of Formula I (in which each of R 1 and R 2 is H, OH, NH 2 , C 1-6 alkyl, C 2-6 alkenyl, optionally N-alkylated C 1-6 aminoalkyl, cycloalkyl, hydroxyalkyl or piperidino or R 1 and R 2 together represent a C 4-7 alkylene radical which can be interrupted by an oxygen or sulphur atom or an imino, alkylimino or arylimino radical and Z represents two hydrogen atoms or a C 2-6 alkylidene radical) and pharmacologically compatible acid addition salts thereof, are prepared by reacting a reactive derivative of a carboxylic acid of the Formula II with a compound of formula R 1 -NH-R 2 and optionally converting the product obtained into a pharmacologically compatible acid addition salt. 2<SP>1</SP>,3<SP>1</SP> - o - Isopropylidene - adenosine - 5<SP>1</SP> - carboxylic acid chloride is prepared by reacting the corresponding acid with thionyl chloride. Pharmaceutical compositions for oral or parenteral administration, comprise a compound of Formula I or a pharmacologically acceptable acid addition salt thereof, together with a pharmaceutical carrier or diluent. The active compounds exhibit a strong circulatory activity.
GB1295228D 1970-07-14 1971-07-08 Expired GB1295228A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19702034785 DE2034785A1 (en) 1970-07-14 1970-07-14 Adenosine 5 carboxylic acid derivatives

Publications (1)

Publication Number Publication Date
GB1295228A true GB1295228A (en) 1972-11-08

Family

ID=5776675

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1295228D Expired GB1295228A (en) 1970-07-14 1971-07-08

Country Status (16)

Country Link
AT (1) AT306253B (en)
AU (1) AU449293B2 (en)
CA (1) CA1077931A (en)
CH (1) CH556345A (en)
DE (1) DE2034785A1 (en)
ES (1) ES393022A1 (en)
FI (1) FI54316C (en)
FR (1) FR2100901B1 (en)
GB (1) GB1295228A (en)
HU (1) HU162216B (en)
IE (1) IE35535B1 (en)
IL (1) IL37280A (en)
NL (1) NL7109584A (en)
SE (1) SE378604B (en)
YU (1) YU34533B (en)
ZA (1) ZA714483B (en)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1082695A (en) * 1972-04-10 1980-07-29 Francis E. Fischer Process for preparing adenosine-5'-carboxamides
US3853846A (en) * 1973-02-12 1974-12-10 Abbott Lab INOSINE-5 -Carboxylates
US3852268A (en) * 1973-02-12 1974-12-03 Abbott Lab Inosine-5 -carboxylic acid amides
US3855206A (en) * 1973-04-11 1974-12-17 Abbott Lab Adenosine-5{40 -carbohydroxamic esters
US3966917A (en) * 1974-07-30 1976-06-29 Abbott Laboratories Platelet aggregation inhibitors
AT350735B (en) * 1976-08-06 1979-06-11 Hoffmann La Roche METHOD FOR PRODUCING NEW RIBO-FURANOSYL IMIDAZOLE DERIVATIVES
US4479942A (en) * 1981-08-10 1984-10-30 Fujisawa Pharmaceutical Co., Ltd. Tetrahydrofurnancarboxylic acid derivatives, processes for preparation thereof and pharmaceutical compositions thereof
US5278150A (en) * 1992-04-24 1994-01-11 Whitby Research, Inc. 2-hydrazoadenosines and their utility for the treatmeat of vascular conditions
TW528755B (en) 1996-12-24 2003-04-21 Glaxo Group Ltd 2-(purin-9-yl)-tetrahydrofuran-3,4-diol derivatives
YU44900A (en) 1998-01-31 2003-01-31 Glaxo Group Limited 2-(purin-9-yl)-tetrahydrofuran-3,4-diol derivatives
PE20060272A1 (en) 2004-05-24 2006-05-22 Glaxo Group Ltd (2R, 3R, 4S, 5R, 2'R, 3'R, 4'S, 5'S) -2.2 '- {TRANS-1,4-CYCLOHEXANODIYLBIS- [IMINO (2 - {[2- (1-METHYL- 1H-IMIDAZOL-4-IL) ETHYL] AMINO} -9H-PURIN-6,9-DIYL)]} BIS [5- (2-ETHYL-2H-TETRAZOLE-5-IL) TETRAHYDRO-3,4-FURANODIOL] AS AN A2A AGONIST
GB0514809D0 (en) 2005-07-19 2005-08-24 Glaxo Group Ltd Compounds

Also Published As

Publication number Publication date
SU385448A3 (en) 1973-05-29
FR2100901A1 (en) 1972-03-24
ES393022A1 (en) 1973-08-01
DE2034785A1 (en) 1972-01-20
YU183371A (en) 1979-02-28
IE35535L (en) 1972-01-14
FR2100901B1 (en) 1974-11-15
FI54316B (en) 1978-07-31
HU162216B (en) 1973-01-29
FI54316C (en) 1978-11-10
AU449293B2 (en) 1974-06-06
IE35535B1 (en) 1976-03-18
SE378604B (en) 1975-09-08
AU3115971A (en) 1973-01-18
ZA714483B (en) 1972-04-26
AT306253B (en) 1973-04-10
NL7109584A (en) 1972-01-18
IL37280A0 (en) 1971-10-20
CH556345A (en) 1974-11-29
IL37280A (en) 1974-03-14
CA1077931A (en) 1980-05-20
YU34533B (en) 1979-09-10

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Legal Events

Date Code Title Description
PS Patent sealed [section 19, patents act 1949]