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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131457생성일: 2026년 10월 26일

(S)-2-(2-Methoxyethyl)piperazine → (S)-7-Chloro-10-[3-(2-methoxy-ethyl)-piperazin-1-yl]-2-methyl-4H-3-thia-4,9-diaza-benzo[f]azulene

https://huagongshe.com/reaction/131457

반응식

참여 물질

역할이름HCID투입량
반응물(S)-2-(2-Methoxyethyl)piperazineHCID 55287560—
반응물7-chloro-2-methyl-4H-3-thia-4,9-diaza-benzo[f]azulen-10-ylamine hydrochlorideHCID 136388572—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
용매Dimethylsulfoxide tolueneHCID 22340214—
생성물(S)-7-Chloro-10-[3-(2-methoxy-ethyl)-piperazin-1-yl]-2-methyl-4H-3-thia-4,9-diaza-benzo[f]azuleneHCID 13609036160%

반응 조건

온도130 °C

반응 단계

Dissolve 7-chloro-2-methyl-4H-3-thia-4,9-diaza-benzo[f]azulen-10-ylamine hydrochloride (1.46 g, 4.86 mmol) and (S)-2-(2-methoxy-ethyl)-piperazine (2.1 g, 14.6 mmol) in dimethylsulfoxide/toluene (1:2)(18 ml), stir under nitrogen and heat in an oil bath at 130° C. for 28.5 hours. Stir 16 hours at ambient temperature. Dilute the mixture with water and ethyl acetate, and extract with ethyl acetate. Combine the ethyl acetate extracts, wash with water and brine, dry the organic phase (Na2SO4), filter and concentrate under reduced pressure. Chromatograph on silica gel (eluent: 0-10% 2N ammonia in methanol/dichloromethane) to give the title compound (1.14 g, 60%), Mass Spectrum (ESMS) 391/393 (M+1), mp 179-183° C. (dec).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07384934B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-0de79bc9bdcf4decb9130433baa099b5
출처 메모uspto-grants-2008_06