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Title:
METHODS FOR PREPARING 2-ALKYNYLADENOSINE DERIVATIVES
Document Type and Number:
WIPO Patent Application WO2004104017
Kind Code:
A3
Abstract:
Disclosed are methods for preparing 2-alkynyladenosine derivatives of Formula (A): or a stereoisomer, pharmaceutically acceptable salt, hydrate, solvate, acid salt hydrate or isomorphic crystalline form thereof, the method comprising the step ofcontacting 2-iodoadenosine-5'-N-ethyluronamide with a compound of Formula (B): wherein Z is -C(=O)OR or -CH20C(=O)R, where R is a C1 to C5 alkyl, preferably methyl. The methods are useful for preparing 2­-alkynyladenosine derivatives that are, in certain embodiments, adenosine receptor agonists.

Inventors:
PICKERSGILL IAIN FRASER (US)
CHEESMAN EDWARD HOLLISTER (US)
Application Number:
PCT/US2004/015783
Publication Date:
March 24, 2005
Filing Date:
May 19, 2004
Export Citation:
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Assignee:
BRISTOL MEYERS SQUIBB PHARMA C (US)
PICKERSGILL IAIN FRASER (US)
CHEESMAN EDWARD HOLLISTER (US)
International Classes:
C07H19/00; C07H19/16; (IPC1-7): C07H19/16
Domestic Patent References:
WO2003029264A22003-04-10
Other References:
J.B. EPP, T.S. WIDLANSKI: "Facile preparation of nucleoside-5'-carboxylic acids", J. ORG. CHEM., vol. 64, 1999, pages 293 - 295, XP002300132
R. MALACHOWSKI ET AL.: "Untersuchungen in der Cyclohexangruppe", CHEM. BER., vol. 71, 1938, pages 759 - 767, XP002300305
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