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HRID 378895作成日:2026年10月26日

Potassium Carbonate → (4-Bromo-2-methyl-phenyl)-(5,11-dihydro-pyrido[2,3-b][1,5]benzodiazepin-6-yl)-methanone

https://huagongshe.com/reaction/378895

反応式

関与物質

役割名称HCID仕込み量
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-methylbenzoyl chlorideHCID 12846483—
溶媒DimethylformamideHCID 6228—
溶媒DiethylformamideHCID 12051—
生成物(4-Bromo-2-methyl-phenyl)-(5,11-dihydro-pyrido[2,3-b][1,5]benzodiazepin-6-yl)-methanoneHCID 1554704953.4%

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 was added solid potassium carbonate (6.3 g, 45.6 mmol). A solution of the crude 4-bromo-2-methylbenzoyl chloride (22.8 mmol) in N,N-diethylformamide was added dropwise, and the mixture stirred at room temperature for 15 minutes. Excess potassium carbonate was filtered off, the filtrate was washed with water and the aqueous layer was extracted with chloroform. The extracts were dried over anhydrous sodium sulfate, evaporated to dryness and the residue dissolved in dichloromethane and absorbed onto a silica Merck-60 flash column. Elution with 20% ethyl acetate in hexane provided the title compound (3.2 g) as a foam which crystallized upon sonication from ethanol hexane.

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-15891177812a46ce937adeb4342eb50b
出典メモuspto-grants-2001_10