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HRID 378897作成日:2026年10月26日

Water → (4-Bromo-2-chloro-phenyl)-(5,11-dihydro-pyrido [2,3-b][1,5] benzodiazepin-10-yl)-methanone

https://huagongshe.com/reaction/378897

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Potassium CarbonateHCID 11430—
反応物6,11-dihydro-5H-pyrido[2,3-b][1,5]benzodiazepineHCID 11030760—
反応物4-Bromo-2-chlorobenzoyl chlorideHCID 15592207—
溶媒DimethylformamideHCID 6228—
生成物(4-Bromo-2-chloro-phenyl)-(5,11-dihydro-pyrido [2,3-b][1,5] benzodiazepin-10-yl)-methanoneHCID 2169687353.9%

反応手順

To a solution of 6,11-dihydro-5H-pyrido[2,3-b][1,5] benzodiazepine (3 g, 15.2 mmol) in N,N-dimethylformamide under nitrogen were added solid potassium carbonate (6.3 g, 45.6 mmol). The mixture was treated dropwise with a solution of the crude 4-bromo-2-chlorobenzoyl chloride (22.9 mmol) in N,N-dimethylformamide. After stirring at room temperature for 15 minutes, water was added under stirring. The resulting solid was collected, dissolved in chloroform, and the solution washed with 1N NaOH and brine. The organic layer was dried over anhydrous sodium sulfate and evaporated to dryness. The residue (purple foam) was dissolved in dichloromethane and absorbed onto a silica Merck-60 flash column. Elution with 20% ethyl acetate in hexane provided 3.4 g of the title compound as a foam which crystallized as a white solid by trituration from ethanol-ether, m.p. 165-168° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06297234B1
出典データセットuspto-grants-2001_10
ORD IDord-cbe60203604a4ead849d41dddccd377c
出典メモuspto-grants-2001_10