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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 325884생성일: 2026년 10월 26일

Phosgene → 5,10-Dihydro-5-{[(1-methyl-4-piperidinyl)oxy]carbonyl}-11H-dibenzo[b,e][1,4]diazepin-11-one

https://huagongshe.com/reaction/325884

반응식

참여 물질

역할이름HCID투입량
반응물PhosgeneHCID 6371—
반응물Sodium CarbonateHCID 10340—
반응물4-Piperidinol, 1-methyl-HCID 66048—
반응물5,10-Dihydro-11H-dibenzo(b,e)(1,4)diazepin-11-oneHCID 201327—
용매TolueneHCID 1140—
용매1,4-DioxaneHCID 31275—
생성물5,10-Dihydro-5-{[(1-methyl-4-piperidinyl)oxy]carbonyl}-11H-dibenzo[b,e][1,4]diazepin-11-oneHCID 13276748—

반응 단계

A quantity of 4.9 gm (0.0425 mol) of 1-methyl-4-piperidinol was added dropwise to a mixture of 22.5 ml of a 20% solution of phosgene in toluene, 100 ml of dioxane, and 4.75 gm (0.045 mol) of anhydrous sodium carbonate while external cooling with ice was carried out. The mixture was stirred for a further 60 minutes at ambient temperature, 9.0 gm (0.0428 mol) of 5,10-dihydro-11H-dibenzo[b,e][1,4]diazepin-11-one were added to the reaction mixture, and this was then refluxed for four hours. The mixture was filtered, the filtrate was concentrated by evaporation in vacuo, and the crude product obtained was purified by column chromatography on 500 gm of silica gel [eluant: ethyl acetate/methanol (volume ratio of 10:1)]. After recrystallization from ethyl acetate, the resulting colorless crystals melted at 203°-204° C. and were identical--according to the mixed melting point, thin layer chromatogram, and IR spectrum--to a product prepared according to Example 4. Yield: 7.6 gm (51% of theory).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04443452
출처 데이터셋uspto-grants-1984_04
ORD IDord-0175f5fc7cb344e9ae00fa40432413e2
출처 메모uspto-grants-1984_04