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HRID 15596作成日:2026年10月24日

4-Fluorobenzoyl chloride → {5-[Benzyl-(4-fluoro-benzoyl)-amino]-2-propyl-benzoimidazol-1-yl}-acetic acid tert-butyl ester

https://huagongshe.com/ja/reaction/15596

反応式

関与物質

役割名称HCID仕込み量
反応物4-Fluorobenzoyl chlorideHCID 67879—
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-(4-fluoro-benzoyl)-amino]-2-propyl-benzoimidazol-1-yl}-acetic acid tert-butyl esterHCID 67200511—

反応手順

4-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-1d181c31d88b400c8195482a3b41f409
出典メモuspto-grants-2010_06