(WO/2002/024625) PROCESS FOR THE PREPARATION OF 3-ARYL-2-HYDROXY PROPANOIC ACID DERIVATIVES

(WO/2002/024625) PROCESS FOR THE PREPARATION OF 3-ARYL-2-HYDROXY PROPANOIC ACID DERIVATIVES

Latest bibliographic data on file with the International Bureau
Pub. No.:  WO/2002/024625   International Application No.:  PCT/IB2001/001699
Publication Date:28.03.2002 International Filing Date:17.09.2001
Chapter 2 Demand Filed: 19.04.2002
IPC: C07C 67/00 (2006.01), C07C 67/10 (2006.01), C07C 67/11 (2006.01)
Applicants:DR. REDDY'S RESEARCH FOUNDATION [IN/IN]; 7-1-27, Ameerpet, Hyderabad 500 016 (IN) (All Except US).
POTLAPALLY, Rajender, Kumar [IN/IN]; (IN) (US Only).
SIRIPRAGADA, Mahender, Rao [IN/IN]; (IN) (US Only).
KOTRA, Narasimha, Murthy [IN/IN]; (IN) (US Only).
SIRISILLA, Raju [IN/IN]; (IN) (US Only).
MAMILLAPALLI, Ramabhadra, Sarma [IN/IN]; (IN) (US Only).
GADDAM, Om, Reddy [IN/IN]; (IN) (US Only).
Inventors:POTLAPALLY, Rajender, Kumar; (IN).
SIRIPRAGADA, Mahender, Rao; (IN).
KOTRA, Narasimha, Murthy; (IN).
SIRISILLA, Raju; (IN).
MAMILLAPALLI, Ramabhadra, Sarma; (IN).
GADDAM, Om, Reddy; (IN).
Priority Data:
795/MAS/2000 22.09.2000 IN
09/836,559 17.04.2001 US
Title: PROCESS FOR THE PREPARATION OF 3-ARYL-2-HYDROXY PROPANOIC ACID DERIVATIVES
Abstract: The present invention relates to an improved process for the preparation of 3-aryl-2-hydroxy propanoic acid derivatives of formula (1) where R?1¿ represents hydrogen atom or (C¿1?-C¿6?)alkyl group and R?2¿ represents (C¿1?-C¿6?)alkyl group which comprises: (i) selectively benzylating L-tyrosine to yield compound of formula (15); (ii). diazotising the compound of formula (15) to produce compound of formula (8); (iii) simultaneous etherification and esterification of compound of formula (8) to obtain crude compound of formula (9) with ee>90 %; (iv) hydrolysing the crude compound of formula (9) to produce compound of formula (9a) acid; (v) treating the compound of formula (9a) with chiral base to produce pure salt of formula (16); (vi) converting the compound of formula (16) to pure compound of formula (9a); (vii) esterifying pure compound of formula (9a) to produce pure compound of formula (9); (viii) debenzylating the compound of formula (9) to yield pure compound of formula (1).
Designated States: AE, AG, AL, AM, AT, AU, AZ, BA, BB, BG, BR, BY, BZ, CA, CH, CN, CO, CR, CU, CZ, DE, DK, DM, DZ, EC, EE, ES, FI, GB, GD, GE, GH, GM, HR, HU, ID, IL, IN, IS, JP, KE, KG, KP, KR, KZ, LC, LK, LR, LS, LT, LU, LV, MA, MD, MG, MK, MN, MW, MX, MZ, NO, NZ, PH, PL, PT, RO, RU, SD, SE, SG, SI, SK, SL, TJ, TM, TR, TT, TZ, UA, UG, US, UZ, VN, YU, ZA, ZW.
African Regional Intellectual Property Org. (ARIPO) (GH, GM, KE, LS, MW, MZ, SD, SL, SZ, TZ, UG, ZW)
Eurasian Patent Organization (EAPO) (AM, AZ, BY, KG, KZ, MD, RU, TJ, TM)
European Patent Office (EPO) (AT, BE, CH, CY, DE, DK, ES, FI, FR, GB, GR, IE, IT, LU, MC, NL, PT, SE, TR)
African Intellectual Property Organization (OAPI) (BF, BJ, CF, CG, CI, CM, GA, GN, GQ, GW, ML, MR, NE, SN, TD, TG).
Publication Language:English (EN)
Filing Language:English (EN)

PATENTSCOPE®

Related Links

E-Newsletters