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HRID 355878作成日:2026年10月26日

Iminodibenyl → N-[4-(10,11-Dihydro-dibenzo[b,f]azepine-5-carbonyl)-phenyl]-2-methyl-benzamide

https://huagongshe.com/reaction/355878

反応式

関与物質

役割名称HCID仕込み量
反応物IminodibenylHCID 10308—
反応物Sodium hydrideHCID 24758—
反応物4-[(2-methylbenzoyl)amino]benzoyl ChlorideHCID 10707441—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒WaterHCID 962—
溶媒PyridineHCID 1049—
溶媒DichloromethaneHCID 6344—
生成物N-[4-(10,11-Dihydro-dibenzo[b,f]azepine-5-carbonyl)-phenyl]-2-methyl-benzamideHCID 153079673.2%

反応条件

温度80 °C

反応手順

To a mixture of 1.37 g (5 mmol) of 4-[(2-methylbenzoyl)amino]benzoyl chloride and 0.061 g of 4-(dimethylamino)pyridine in 4 ml of pyridine is added 0.975 g (5 mmol) of 10,11-dihydro-5H-dibenz[b,f]azepine. The mixture is heated at 80° C. for 18 hours and then 0.2 g of sodium hydride (60% in oil) (5 mmol) is added. The mixture is refluxed for 2 hours, diluted with dichloromethane and water and then filtered. To the filtrate is added 1N HCl and the mixture filtered. The filtrate is dried (Na2 SO4) and the solvent removed to give a solid. The solid (1.1 g) is chromatographed on thick layer silica gel plates to give 70 mg of yellow solid, m.p. 112°-118° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05834461
出典データセットuspto-grants-1998_11
ORD IDord-5f309f1249e14c1b99ecad4da7649a8b
出典メモuspto-grants-1998_11