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【结 构 式】

【分子编号】37013

【品名】methyl 4-[5-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-quinoxalinyl)-1H-pyrrol-2-yl]benzoate

【CA登记号】

【 分 子 式 】C24H27N3O2

【 分 子 量 】389.4974

【元素组成】C 74.01% H 6.99% N 10.79% O 8.22%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(XIV)

Cyclization of diketone (XII) with ammonium acetate afforded the pyrrole derivative (XIV). The methyl ester group was finally hydrolyzed with NaOH to the target carboxylic acid.

1 Tai, K.; Yamauchi, T.; Hida, T.; Kikuchi, K.; Nagia, M.; Yoshimura, H.; Tokuhara, N.; Hibi, S.; Synthesis and structure-activity relationships of 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-quinoxaline derivatives with retinoic acid receptor alpha agonistic activity. J Med Chem 2000, 43, 3, 409.
2 Kikuchi, K.; Tagami, K.; Yoshimura, H.; Hibi, S.; Nagai, M.; Abe, S.; Okita, M.; Hida, T.; Higashi, S.; Tokuhara, N.; Kobayashi, S. (Eisai Co., Ltd.); Heterocyclic carboxylic acid derivs. and drugs containing the same. JP 1997071566; US 5977108; WO 9702244 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(XII) 37012 methyl 4-[4-oxo-4-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-quinoxalinyl)butanoyl]benzoate C24H28N2O4 详情 详情
(XIV) 37013 methyl 4-[5-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-quinoxalinyl)-1H-pyrrol-2-yl]benzoate C24H27N3O2 详情 详情
Extended Information