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HRID 346450作成日:2026年10月26日

2-Ethylpropanedioyl dichloride → 3-[7-(3-Fluoro-benzyloxy)-1,2,4,5-tetrahydro-benzo[d]azepin-3-yl]-3-oxo-propionamide

https://huagongshe.com/reaction/346450

反応式

関与物質

役割名称HCID仕込み量
反応物2-Ethylpropanedioyl dichlorideHCID 10920924—
反応物7-(3-fluoro-benzyloxy)-2,3,4,5-tetrahydro-1H-benzo[d]azepine hydrochlorideHCID 21080184—
反応物3-[7-(3-Fluoro-benzyloxy)-1,2,4,5-tetrahydro-benzo[d]azepin-3-yl]-3-oxo-propionic acid ethyl esterHCID 69290734—
溶媒TriethylamineHCID 8471—
生成物3-[7-(3-Fluoro-benzyloxy)-1,2,4,5-tetrahydro-benzo[d]azepin-3-yl]-3-oxo-propionamideHCID 1177268370%

反応手順

3-[7-(3-Fluoro-benzyloxy)-1,2,4,5-tetrahydro-benzo[d]azepin-3-yl]-3-oxo-propionic acid ethyl ester: The title compound was prepared in analogy to Example 1d) from 7-(3-fluoro-benzyloxy)-2,3,4,5-tetrahydro-1H-benzo[d]azepine hydrochloride [Example 1c)] and ethyl malonic acid chloride with triethylamine as the base. Yield: 70% of theory as a colourless oil; MS: m/e=386 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07173023B2
出典データセットuspto-grants-2007_02
ORD IDord-0cc9c9d9b5fb4a71ae071e7b3c235fb3
出典メモuspto-grants-2007_02