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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 67228생성일: 2026년 10월 24일

Triethylamine → 2-(o-Chlorophenyl)-3-(3,4-dimethoxyphenyl)-2,3,5,6,7,8-hexahydrothiazolo[3,2-a][1,3]diazepin-3-ol

https://huagongshe.com/ko/reaction/67228

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물1,3-Diazepane-2-thioneHCID 736589—
반응물2-(2-Chlorophenyl)-1-(3,4-dimethoxyphenyl)-2-hydroxyethan-1-oneHCID 15044219—
용매AcetoneHCID 180—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물2-(o-Chlorophenyl)-3-(3,4-dimethoxyphenyl)-2,3,5,6,7,8-hexahydrothiazolo[3,2-a][1,3]diazepin-3-olHCID 13068287—

반응 단계

A 6.13 g. portion of 2'-chloro-3,4-dimethoxybenzoin, 5.6 ml. of triethylamine and 20 ml. of toluene are mixed and stirred. A mixture of 1.55 ml. of methanesulfonyl chloride in 40 ml. of toluene is added over a period of one hour. A 50 ml. portion of water and more toluene are added. The organic layer is separated, washed with water and concentrated in vacuo to give 8.3 g. of 2'-chloro-3,4-dimethoxybenzoin methanesulfonate ester as a viscous oil. A mixture of this oil in 30 ml. of acetone is added to a stirred mixture of 1.95 g. of hexahydro-2H-1,3-diazepine-2-Thione in 150 ml. of acetone. The resulting mixture is stirred for 3 hours, then 3 hours at 45°-50° C., concentrated to 1/3 of its original volume and ether is added producing a gum. The mixture is concentrated free of solvents, 100 ml. of water and 2 ml. of ammonium hydroxide are added and the solid is filtered and washed with water. This solid is dissolved in 20 ml. of ethanol and refrigerated giving 1.3 g. of the desired product, m.p. 98°-100° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04344954
출처 데이터셋uspto-grants-1982_08
ORD IDord-3dd7ab568a7044628a6fc2869f0d7c63
출처 메모uspto-grants-1982_08