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HRID 15600作成日:2026年10月26日

Diisopropylethylamine → {5-[Benzyl-(2,6-difluoro-benzoyl)-amino]-2-propyl-benzoimidazol-1-yl}-acetic acid tert-butyl ester

https://huagongshe.com/reaction/15600

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物2,6-Difluorobenzoyl chlorideHCID 87438—
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-(2,6-difluoro-benzoyl)-amino]-2-propyl-benzoimidazol-1-yl}-acetic acid tert-butyl esterHCID 67199631—

反応手順

2,6-Difluoro-benzoyl chloride (45 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 C30H31F2N3O3+H: 520, observed: 520.

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-286327cbf748443ab88ceffc943922b5
出典メモuspto-grants-2010_06