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【结 构 式】

【分子编号】50659

【品名】benzyl 2-methyl-2-(2-naphthyl)propanoate

【CA登记号】

【 分 子 式 】C21H20O2

【 分 子 量 】304.3886

【元素组成】C 82.86% H 6.62% O 10.51%

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:(III)

The precursor 2,2-dimethyl-(2-naphthyl)acetic acid (IV) was prepared as follows. 2-Naphthylacetic acid (I) was converted to the benzyl ester (II) by treatment with benzyl bromide and DBU. Dimethylation of the sodium enolate of (II) with iodomethane furnished (III). Removal of the benzyl ester group of (III) was then achieved by hydrogenolysis in the presence of Pd/C.

1 Betageri, R.; Llinas-Brunet, M.; Moss, N.; Patel, U.; Cardozo, M.; Beaulieu, P.L.; Ferland, J.-M.; Proudfoot, J.R. (Boehringer Ingelheim Pharmaceuticals Inc.); Pyridones as Src family SH2 domain inhibitors. EP 1045836; US 6054470; US 6156784; WO 9931066 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 50657 2-Naphthylacetic acid; beta-Naphthylacetic acid 581-96-4 C12H10O2 详情 详情
(II) 50658 benzyl 2-(2-naphthyl)acetate C19H16O2 详情 详情
(III) 50659 benzyl 2-methyl-2-(2-naphthyl)propanoate C21H20O2 详情 详情
(IV) 50660 2-methyl-2-(2-naphthyl)propionic acid C14H14O2 详情 详情
Extended Information