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HRID 1715390作成日:2026年10月25日

5-Bromo-2-chlorobenzoic acid → 5-bromo-2-chloro-N-cyclopropylbenzamide

https://huagongshe.com/reaction/1715390

反応式

関与物質

役割名称HCID仕込み量
反応物5-Bromo-2-chlorobenzoic acidHCID 33127—
反応物Oxalyl chlorideHCID 65578—
反応物CyclopropylamineHCID 69828—
反応物DiisopropylethylamineHCID 81531—
触媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物5-bromo-2-chloro-N-cyclopropylbenzamideHCID 480698394%

反応手順

To a suspension of 5-bromo-2-chlorobenzoic acid (17.6 g, 75 mmol) in CH2Cl2 (180 mL) was added oxalyl chloride (7.0 mL, 83 mmol). DMF (8 drops) was added, and the mixture was stirred for 2 h at rt (gas evolution). The mixture was reduced under reduced pressure, and the crude residue was diluted with CH2Cl2 (530 mL). The mixture was cooled to 0° C., and a sol. of cyclopropylamine (5.8 mL, 83 mmol) in CH2Cl2 (45 mL) was added dropwise. The mixture was stirred for 10 min at 0° C., and was allowed to warm to rt. DIPEA (14.3 mL, 84 mmol) was added, and the mixture was stirred for 2 h at rt. The mixture was diluted with more CH2Cl2, and was washed with aq. 10% HCl, water, and brine. The org. layer was dried over MgSO4, filtered, and the solvents were removed under reduced pressure. The residue was triturated with hexane, filtered, and dried under high vacuum to yield the title compound (19.3 g, 94%). LC-MS: tR=0.84 min; ES+: 316.89.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07799805B2
出典データセットuspto-grants-2010_09
ORD IDord-608d607d04c74495800824fbac261fa4
出典メモuspto-grants-2010_09