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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 35112생성일: 2026년 10월 24일

1,2-Dichloroethane → 4-Chloro-6-(4-methyl-1-piperazinyl)-1,2,dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine

https://huagongshe.com/ko/reaction/35112

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참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물N-[2-(5-chloro-1-indolinyl)phenyl]-4-methyl-1-piperazinecarboxamideHCID 13823362—
용매DichloromethaneHCID 6344—
생성물4-Chloro-6-(4-methyl-1-piperazinyl)-1,2,dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepineHCID 1382329529.5%

반응 조건

온도75 °C

반응 단계

To N-[2-(5-chloro-1-indolinyl)phenyl]-4-methyl-1-piperazinecarboxamide (13.5 g, 36.5 mmoles) was added a solution of polyphosphoric acid ethyl ester and 1,2-dichloroethane (250 ml) The solution was heated at 75° C. for 4 hours with exclusion of moisture. The solution was cooled and poured into a mixture of ice-sodium hydroxide solution (2 l) and dichloromethane (1.2 l). The mixture was stirred for 15 minutes. The layers were separated. The organic layer was washed with 2 l of 2N sodium hydroxide, then with brine (500 ml), and dried over anhydrous magnesium sulfate. Removal of the solvent at reduced pressure gave an oil. The oil was purified by flash chromatography on a silica gel column (1 kg, 230-400 mesh), packed and eluted initially with dichloromethane, then with dichloromethane containing an increasing methanol content in 1% increments to a final content of 5% (total 8 l). Concentration of the 5% methanol/dichloromethane eluent gave 3.8 g (28%) of product. Recrystallization from 2-propanol (50 ml) gave the analytical sample, mp 182°-183° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04764616
출처 데이터셋uspto-grants-1988_08
ORD IDord-537b72dbff364460abb2bda845c26835
출처 메모uspto-grants-1988_08