돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32288생성일: 2026년 10월 24일

Dichloromethane → N-(2-diethylamino-ethyl)-4-(2-benzyloxy-acetylamino)-2-methoxy-benzamide

https://huagongshe.com/ko/reaction/32288

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물4-Amino-N-[2-(diethylamino)ethyl]-2-methoxybenzamideHCID 77374—
반응물(Benzyloxy)acetic acidHCID 290301—
용매WaterHCID 962—
생성물N-(2-diethylamino-ethyl)-4-(2-benzyloxy-acetylamino)-2-methoxy-benzamideHCID 5979333727%

반응 조건

온도4 °C

반응 단계

664 mg (4 mmol) of benzyloxyacetic acid is introduced into 20 ml of methylene chloride, mixed with 768 mg (4 mmol) of N′-(3-dimethylaminopropyl)-N-ethylcarbodiimide (EDG), and stirred for 0.5 hour at 4° C. Then, 1.06 g (4 mmol) of 4-amino-N-(2-diethylamino-ethyl)-2-methoxy-benzamide in a total of 12 ml of methylene chloride is added to the batch and stirred for 48 hours at room temperature. After 30 ml of water is added, it is extracted twice with 30 ml each of methylene chloride. The organic phase is dried, filtered and concentrated by evaporation. The residue is chromatographed on 20 g of Isolute NH2 (50 μm) with methylene chloride. The correspondingly combined fractions are concentrated by evaporation and chromatographed again on 20 g of Isolute NH2 (50 μm) with a gradient from cyclohexane to cyclohexane:methylene chloride=50:50 as an eluant, and 348 mg (27% of theory) of N-(2-diethylamino-ethyl)-4-(2-benzyloxy-acetylamino)-2-methoxy-benzamide is obtained as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07427390B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-82caffa4065a4ce5a8a0b285a7b56e7f
출처 메모uspto-grants-2008_09