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HRID 727243作成日:2026年10月25日

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

https://huagongshe.com/reaction/727243

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Sodium hydrideHCID 24758—
反応物5,10-Dihydro-11H-dibenzo(b,e)(1,4)diazepin-11-oneHCID 201327—
溶媒DimethylformamideHCID 6228—
生成物11H-Dibenzo(b,e)(1,4)diazepin-11-one, 5,10-dihydro-10-methyl-HCID 3604263%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05712292
出典データセットuspto-grants-1998_01
ORD IDord-83ecdd1848e440c79cb7d392ef7810cf
出典メモuspto-grants-1998_01