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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 67237생성일: 2026년 10월 23일

2-Chlorobenzaldehyde → 2-(o-Chlorophenyl)-2,3,5,6,7,8-hexahydro-3-(2-thienyl)-thiazolo[3,2-a][1,3]diazepin-3-ol

https://huagongshe.com/ko/reaction/67237

반응식

참여 물질

역할이름HCID투입량
반응물2-ChlorobenzaldehydeHCID 6996—
반응물2-ThiophenecarboxaldehydeHCID 7364—
반응물Potassium CyanideHCID 9032—
반응물Methanesulfonyl chlorideHCID 31297—
반응물1,3-Diazepane-2-thioneHCID 736589—
용매AcetoneHCID 180—
용매EthanolHCID 702—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매TriethylamineHCID 8471—
생성물2-(o-Chlorophenyl)-2,3,5,6,7,8-hexahydro-3-(2-thienyl)-thiazolo[3,2-a][1,3]diazepin-3-olHCID 13068309—

반응 단계

A mixture of 9.2 ml. of 2-thiophenecarboxaldehyde, 11.3 ml. of o-chlorobenzaldehyde, 8 g. of potassium cyanide and 100 ml. of 65% ethanol is refluxed for 2 hours and then refrigerated. A 30 ml. portion of water is added, refrigeration is continued, the oil is separated by decantation, added to toluene, washed with water, dried and concentrated giving 12.7 g. of an oil. A 9.0 g. portion of this oil is mixed with 8.4 ml. of triethylamine and 100 ml. of toluene and stirred as a mixture of 2.4 ml. of methanesulfonyl chloride in 100 ml. of toluene is added. The mixture is stirred overnight then 100 ml. of water is added. The toluene layer is separated, washed with water, dried and concentrated, giving 10.6 g. of oily 2-thienyl α-hydroxy(2-chlorophenyl)ketone. This oil is combined with 3.9 g. of hexahydro-2H-1,3-diazepin-2-thione in 150 ml. of acetone and allowed to stand 48 hours. The solvent is removed, 100 ml. of water and 2 ml. of ammonium hydroxide are added and the aqueous layer is decanted. Ethanol is added, the mixture is cooled and the solid is collected, giving 3.4 g. of the desired product, m.p. 120°-122° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04344954
출처 데이터셋uspto-grants-1982_08
ORD IDord-1ac4433c53b549cab3064718b77f2db4
출처 메모uspto-grants-1982_08