作者:K. G. Grozinger、V. Fuchs、K. D. Hargrave、S. Mauldin、J. Vitous、S. Campbell、J. Adams
DOI:10.1002/jhet.5570320144
日期:1995.1
Several synthetic methods were developed during the process optimization for the large scale synthesis of nevirapine (1), a non-nucleoside inhibitor of HIV-1 Reverse Transcriptase. The synthesis of its putative major metabolite 11-cyclopropyl-5,11-dihydro-4-hydroxymethyl-6H-[3,2-b:2′,3′-e][1,4]diazepin-6-one (2) and the oxidation of 2 to the corresponding aldehyde 3, are described.
在工艺优化过程中开发了几种合成方法,用于大规模合成奈韦拉平(1),这是一种HIV-1逆转录酶的非核苷抑制剂。推定的主要代谢物11-环丙基-5,11-二氢-4-羟甲基-6 H- [3,2- b:2',3'- e ] [1,4]二氮杂6-1-6(2)和氧化2成相应的醛3,中有描述。