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HRID 529648作成日:2026年10月27日

Triethylamine → 4-Amino-3-chloro-N,N-dimethylbenzamide

https://huagongshe.com/reaction/529648

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Dimethylamine, hydrochlorideHCID 10473—
反応物4-Amino-3-chlorobenzoic acidHCID 17211—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
溶媒IsopropanolHCID 3776—
溶媒ChloroformHCID 6212—
溶媒DichloromethaneHCID 6344—
生成物4-Amino-3-chloro-N,N-dimethylbenzamideHCID 2028748159.6%

反応手順

To a solution of 4-amino-3-chloro-benzoic acid (1 equiv) in DCM (0.12 M) was added N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (1.2 equiv), 1-hydroxybenzotriazole (1.2 equiv), triethylamine (4 equiv) and dimethylamine hydrochloride (2 equiv) sequentially. The mixture was stirred at room temperature overnight. After the reaction was complete, as monitored by LCMS, the mixture was diluted with a mixture of isopropanol in chloroform (30%,), washed with water and dried over anhydrous sodium sulfate. The organic phase was concentrated and the residue obtained was recrystallized in the mixture of hexane and ethyl acetate (10%,) to afford the desired product (Yield: 59.6%) as a light brown solid. MS (ESI) m/z 199.1 [M+1]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09346812B2
出典データセットuspto-grants-2016_05
ORD IDord-0187656467444a3f8b52cea66baa6d74
出典メモuspto-grants-2016_05