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HRID 15592作成日:2026年10月26日

2-Fluorobenzoyl chloride → {5-[Benzyl-(2-fluoro-benzoyl)-amino]-2-propyl-benzoimidazol-1-yl}-acetic acid tert-butyl ester

https://huagongshe.com/reaction/15592

反応式

関与物質

役割名称HCID仕込み量
反応物2-Fluorobenzoyl chlorideHCID 9808—
反応物DiisopropylethylamineHCID 81531—
反応物(5-Benzylamino-2-propyl-benzoimidazol-1-yl)-acetic acid tert-butyl esterHCID 67200053—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒Hydrochloric AcidHCID 313—
溶媒DichloromethaneHCID 6344—
生成物{5-[Benzyl-(2-fluoro-benzoyl)-amino]-2-propyl-benzoimidazol-1-yl}-acetic acid tert-butyl esterHCID 67199918—

反応手順

2-Fluoro-benzoyl chloride (42 μL, 0.36 mmol) was added to a solution of (5-benzylamino-2-propyl-benzoimidazol-1-yl)-acetic acid tert-butyl ester (45 mg, 0.12 mmol), DIEA (41 μL, 0.24 mmol) and DMAP (15 mg, 0.12 mmol) in CH2Cl2 (1 mL), and stirred overnight at room temperature. The reaction solution was diluted with aqueous HCl (1.0 M) and filtered through an Extrelut column. The Extrelut column was washed with CH2Cl2, and the filtrate was concentrated to afford the subtitle compound that was used without further purification. MS calculated for C30H32FN3O3+H: 502, observed: 502.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732618B2
出典データセットuspto-grants-2010_06
ORD IDord-1754c8e370c345a2817119b79bdd21ba
出典メモuspto-grants-2010_06