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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4021생성일: 2026년 10월 23일

Water → N-[5-bromo-2-(2,3-dihydro-1H-indol-1-yl)phenyl]-N',N'-dimethylurea

https://huagongshe.com/ko/reaction/4021

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Dimethylcarbamoyl ChlorideHCID 6598—
반응물Sodium BicarbonateHCID 516892—
반응물1-(2-Amino-4-bromophenyl)indoline hydrochlorideHCID 13823321—
용매ChloroformHCID 6212—
생성물N-[5-bromo-2-(2,3-dihydro-1H-indol-1-yl)phenyl]-N',N'-dimethylureaHCID 1382336940.3%

반응 단계

To a stirred mixture, under nitrogen, of 28.9 g (0.10 mole) of 1-(2-amino-4-bromophenyl)indoline hydrochloride and 16.8 g (0.20 mole) of anhydrous powdered sodium bicarbonate in 500 ml of chloroform was added a solution of 21.5 g (0.20 mole) of dimethylcarbamyl chloride in 25 ml of chloroform, over a 10 minute period. The mixture was heated under reflux for 7 hours, and 8.4 g (0.10 mole) of sodium bicarbonate and 10.7 g (0.10 mole) of the dimethylcarbamyl chloride were added. After heating under reflux for 2 days, equivalent amounts (8.4 g of sodium bicarbonate and 10.7 g of dimethylcarbamyl chloride) were added. After three days under reflux, the mixture was cooled and 500 ml of water was added. The phases were stirred vigorously for 0.5 hours and separated. The organic phase was washed three times with water, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was dissolved in 200 ml of dichloromethane and adsorbed on a chromatography column containing 1 kg of silica gel packed in and eluted with dichloromethane. The fractions containing product were combined and concentrated to afford 14.5 g (40%) of product. Recrystallization from toluene (charcoal)/hexane gave the analytical sample, mp 119°-121° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04723007
출처 데이터셋uspto-grants-1988_02
ORD IDord-bdf54aa101ac42ae9c74e2e30e8f117d
출처 메모uspto-grants-1988_02