돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 275490생성일: 2026년 10월 26일

Oxamic Acid → N-[2-(3-Cyclopentyloxy-4-methoxyphenyl)ethyl]oxamide

https://huagongshe.com/reaction/275490

반응식

참여 물질

역할이름HCID투입량
반응물Oxamic AcidHCID 974—
반응물4-MethylmorpholineHCID 7972—
반응물Ethyl chloroformateHCID 10928—
반응물Ammonium ChlorideHCID 25517—
반응물3-Cyclopentyloxy-4-methoxyphenethylamineHCID 11276394—
용매1,2-DimethoxyethaneHCID 8071—
생성물N-[2-(3-Cyclopentyloxy-4-methoxyphenyl)ethyl]oxamideHCID 986134830%

반응 단계

To a suspension of oxamic acid (1.76 g, 20 mmol) in 1,2-dimethoxyethane (75 mL) under an argon atmosphere was added dropwise N-methylmorpholine (2.55 mL, 23 mmol) followed by ethyl chloroformate (2.20 mL, 23 mmol). After stirring for 1 h at room temperature, a solution of 2-(3-cyclopentyloxy-4-methoxy-phenyl)ethylamine (4.65 g, 20 mmol) in 1,2-dimethoxyethane (30 mL) was added over 5 min, and the resulting mixture was stirred for 2 h. Saturated aqueous ammonium chloride was added and the solvent was removed under reduced pressure. The solid residue was dissolved in methanol/methylene chloride, washed successively with water, 10% hydrochloric acid, aqueous sodium bicarbonate and water and dried (potassium carbonate). The solvent was removed in vacuo and the residue was purified by flash chromatography, eluting with 1% i-propanol/methylene chloride to provide the oxamide (1.82 g, 30%): m.p. 175°-175.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05393788
출처 데이터셋uspto-grants-1995_02
ORD IDord-11799f87b34444998fe8615eefb7b91c
출처 메모uspto-grants-1995_02