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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 727243생성일: 2026년 10월 24일

Methyl iodide → 11H-Dibenzo(b,e)(1,4)diazepin-11-one, 5,10-dihydro-10-methyl-

https://huagongshe.com/ko/reaction/727243

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물5,10-Dihydro-11H-dibenzo(b,e)(1,4)diazepin-11-oneHCID 201327—
용매DimethylformamideHCID 6228—
생성물11H-Dibenzo(b,e)(1,4)diazepin-11-one, 5,10-dihydro-10-methyl-HCID 3604263%

반응 단계

To a solution of 11-oxo-10,11-dihydro-5H-dibenzo[b,e][1,4]diazepine (10 g, 0.048 mol, Synthesis, (1985), 550) in dry dimethylformamide (100 ml) kept under an atmosphere of nitrogen, sodium hydride (2.1 g, 0.052 mol, 60% dispersion in oil) was added, and the reaction mixture was stirred for 1.5 h. Iodomethane (3.27 ml, 0.052 mol) was slowly added keeping the temperature below 30° C. and the mixture was stirred overnight. The reaction mixture was quenched with saturated ammonium chloride (20 ml) and poured onto ice water (300 ml). The solid was filtered off and washed with plenty of water and dried. This yielded 10.4 g of crude 10-methyl-11-oxo-10,11-dihydro-5H-dibenzo[b,e][1,4]diazepine which was recrystallised from methanol (200 ml), to give 6.7 g (63%) of 10-methyl-11-oxo-10,11-dihydro-5H-dibenzo[b,e][1,4]diazepine. M.p. 210°-211° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05712292
출처 데이터셋uspto-grants-1998_01
ORD IDord-83ecdd1848e440c79cb7d392ef7810cf
출처 메모uspto-grants-1998_01