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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 436135생성일: 2026년 10월 25일

Hydrochloric Acid → 9-(3-Dimethylamino-2-methylpropyl)-4,9-dihydro-4-methyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-one, hydrochloride

https://huagongshe.com/reaction/436135

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium hydrideHCID 24758—
반응물3-Chloro-2-methylpropyl(dimethyl)ammonium chlorideHCID 3083841—
반응물HCID 12521642HCID 12521642—
용매Diethyl EtherHCID 3283—
용매DimethylformamideHCID 6228—
생성물9-(3-Dimethylamino-2-methylpropyl)-4,9-dihydro-4-methyl-10H-thieno[3,4-b][1,5]benzodiazepin-10-one, hydrochlorideHCID 131710151—

반응 단계

A mixture of 0.47 g. of 55% sodium hydride-mineral oil dispersion and 0.91 g. of 3-dimethylamino-2-methylpropylchloride hydrochloride in 35 ml. of dry dimethylformamide is stirred at room temperature for 0.5 hours. To the mixture is added 0.6 g. of 4,9-dihydro-4-methyl-10H-thieno[3,4-b][1,5]-benzodiazepin-10-one and stirring is continued for 18 hours. The reaction mixture is cooled, quenched with water and extracted with chloroform. The dried chloroform extracts are concentrated to an oil, which is chromatographed on silica gel preparative thin layer chromatographic (tlc) plates with 10:1 benzene:methanol to give an oil. An ethanolic solution of the oil is treated with anhydrous hydrogen chloride and diluted with ether to give a white solid, m.p. 231°-233° C. (dec.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04007272
출처 데이터셋uspto-grants-1977_02
ORD IDord-fba65642a3c44c77a2a1b653bd2ba640
출처 메모uspto-grants-1977_02