Process development and scale-up of a selective α1-adrenoceptor antagonist

被引:17
作者
Connolly, TJ [1 ]
Matchett, M [1 ]
Sarma, K [1 ]
机构
[1] Roche Palo Alto LLC, NCD Chem Serv, Chem Dev, Palo Alto, CA 94304 USA
关键词
D O I
10.1021/op0498114
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A synthetic route to a potent and selective a-l-adrenergic receptor antagonist has been developed and demonstrated in a pilot plant. The route has been used in two pilot plant campaigns and has produced RO3203546 in 2.3 and 12.0 kg batch sizes. The first pilot plant campaign focused primarily on the end-game of the process with particular emphasis on the development of a method to isolate the active pharmaceutical ingredient (API). The second pilot plant campaign allowed front-end process improvements to be demonstrated. The reiterative process improvements resulted in an economical process with improved throughput and product quality when compared to the original discovery synthesis.
引用
收藏
页码:80 / 87
页数:8
相关论文
共 6 条
[1]  
CAINE M, 1976, BRIT J UROL, V48, P255, DOI 10.1111/j.1464-410X.1976.tb03013.x
[2]   ANTIHYPERTENSIVE 2-AMINO-4(3H)-QUINAZOLINONES [J].
HESS, HJ ;
CRONIN, TH ;
SCRIABINE, A .
JOURNAL OF MEDICINAL CHEMISTRY, 1968, 11 (01) :130-+
[3]   Potential toxicological concerns associated with carboxylic acid chlorination and other reactions [J].
Levin, D .
ORGANIC PROCESS RESEARCH & DEVELOPMENT, 1997, 1 (02) :182-182
[4]  
*OSHA PEL, 2004, ULLM ENCY IND CHEM, DOI DOI 10.1002/14356007A08_545_
[5]   Efficient enantioselective synthesis of the NMDA 2B receptor antagonist Ro 67-8867 [J].
Scalone, M ;
Waldmeier, P .
ORGANIC PROCESS RESEARCH & DEVELOPMENT, 2003, 7 (03) :418-425
[6]  
*TLV TWA, 2004, ULLM ENCY IND CHEM, DOI DOI 10.1002/14356007.A10_101