The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.
The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.
Patent No.:
Date of Patent:
May. 29, 2001
Filed:
May. 15, 2000
Attila Kis-Tamás, Budapest, HU;
Csaba Huszár, Budapest, HU;
Bertrand Castro, Aunes, FR;
Attila Németh, Göd, HU;
Péter Aranyosi, Budapest, HU;
Károly Gyüre, Dunakeszi, HU;
István Mészáros, Budapest, HU;
Ilona Dervalicsné Zrínyi, Budapest, HU;
Katalin Dubovszki, Budapest, HU;
Lajosné Páli, Budapest, HU;
Antal Gajáry, Budapest, HU;
Attila Supic, Budapest, HU;
Zsuzsanna Nád, Budapest, HU;
Zoltán Makovi, Budapest, HU;
Endre Kollár, Budapest, HU;
Zsuzsanna Csetriné Hári, Budapest, HU;
Ágnes Kunsztné Kárász, Budapest, HU;
Erzsébet Bognár, Budapest, HU;
Sanofi-Synthelabo, Paris, FR;
Abstract
Process for the preparation of compounds of formula (I) wherein R means hydrogen atom, or C,alkyl group, or C,aralkyl group or phenyl group, characterised in that: a) the compound of formula (III) is reacted with a compound of formula (IV) wherein X means halogen atom or C,alkoxy group or hydroxyl group and the resulting compound of formula (II) is transformed in the presence of an oxidising agent in a reaction medium with pH above 7, into the compound of formula (I), or b) the compound of formula (III) is reacted with an anhydride of general formula (V) and the resulting compound of formula (II) transformed in the presence of an oxidising agent, in a reaction medium with pH above 7, into the compound of formula (I), or c) a compound of formula (II) is transformed in the presence of an oxidising agent, in a reaction medium with pH above 7, into the compound of formula (I), and if desired, the resulting compounds of formula (I), before or after isolation, are transformed into acid addition salts, or the compounds of formula (I) are liberated from their acid addition salts. Thus a process for the preparation of intermediates useful in synthesis of angiotensin II antagonists is disclosed.