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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 67229생성일: 2026년 10월 24일

Methanesulfonyl chloride → 2,3,5,6,7,8-Hexahydro-3-(5-methyl-2-thienyl)-2-phenylthiazolo[3,2-a][1,3]diazepin-3-ol

https://huagongshe.com/ko/reaction/67229

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonyl chlorideHCID 31297—
반응물1,3-Diazepane-2-thioneHCID 736589—
반응물5-Methyl-2-thienyl-alpha-hydroxybenzyl ketoneHCID 53958387—
용매AcetoneHCID 180—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매TriethylamineHCID 8471—
생성물2,3,5,6,7,8-Hexahydro-3-(5-methyl-2-thienyl)-2-phenylthiazolo[3,2-a][1,3]diazepin-3-olHCID 13068288—

반응 단계

A mixture of 1.71 ml. of methanesulfonyl chloride in 40 ml. of toluene is added dropwise to a stirred slurry of 4.65 g. of 5-methyl-2-thienyl-α-hydroxybenzyl ketone and 5.6 ml. of triethylamine in 40 ml. of toluene. The mixture is stirred 20 hours, water is added and the organic layer is separated, washed with water and concentrated to dryness. A 20 ml. portion of ether is added to the residue giving a solid which is collected, washed with ether and dried, giving 4.8 g. of 5-methyl-2-thienyl-α-hydroxybenzyl ketone methanesulfonate ester. A mixture of 2.01 g. of this ester and 0.84 g. of hexahydro-2H-1,3-diazepine-2-thione in 40 ml. of acetone is allowed to stand 48 hours. The solvent is removed, 50 ml. of water and one ml. of concentrated ammonium hydroxide are added and the resulting solid is collected and washed with water. This solid is dissolved in 7 ml. of ethanol and then cooled. The resulting solid is collected, washed with ethanol, then ether and dried in vacuo, giving 1.2 g. of the desired product as a yellow solid, m.p. 70°-90° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04344954
출처 데이터셋uspto-grants-1982_08
ORD IDord-7043d8d5037247b294707004144c7972
출처 메모uspto-grants-1982_08