돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 395808생성일: 2026년 10월 27일

N-(2-Aminophenyl)-4-methoxybenzamide → N1-(4-Methoxybenzoyl)-N2-(5-chlorobenzofuran-2-ylcarbonyl)-1,2-benzenediamine

https://huagongshe.com/reaction/395808

반응식

참여 물질

역할이름HCID투입량
반응물N-(2-Aminophenyl)-4-methoxybenzamideHCID 785232—
반응물5-Chloro-1-benzofuran-2-carboxylic acidHCID 937838—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물N1-(4-Methoxybenzoyl)-N2-(5-chlorobenzofuran-2-ylcarbonyl)-1,2-benzenediamineHCID 2135276660.1%

반응 단계

To a solution of N1-(4-methoxybenzoyl)-1,2-benzenediamine (200 mg, 0.826 mmol) in methylene chloride (5 mL) was added 5-chlorobenzofuran-2-carboxylic acid (162 mg, 0.826 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (316 mg, 1.65 mmol), and 4-dimethylaminopyridine (10 mg, 0.083 mmol), The resulting solution was stirred at room temperature for 6 h. The resulting precipitate was collected via vacuum filtration to provide 209 mg (60%) of the title compound as an amorphous off-white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06605626B2
출처 데이터셋uspto-grants-2003_08
ORD IDord-7d9cc5b1f30945c98294dd9775630341
출처 메모uspto-grants-2003_08