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HRID 342310作成日:2026年10月27日

Dimethylformamide → 1-(2'-Methoxybiphen-4-ylcarbonyl)-5-oxo-2,3,4,5-tetrahydro-1h-1-benzazepine

https://huagongshe.com/reaction/342310

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Oxalyl chlorideHCID 65578—
反応物1,2,3,4-Tetrahydro-benzo(b)azepin-5-oneHCID 294788—
反応物2'-Methoxy-biphenyl-4-carboxylic acidHCID 2759548—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物1-(2'-Methoxybiphen-4-ylcarbonyl)-5-oxo-2,3,4,5-tetrahydro-1h-1-benzazepineHCID 54335813—

反応手順

A 1.67 g portion of 2'-methoxybiphen-4-ylcarboxylic acid was dissolved in 17 ml of dichloromethane, 0.95 ml of oxalyl chloride and a catalytically effective amount of dimethylformamide were added to the resulting solution with cooling on an ice bath and then the resulting mixture was warmed up to room temperature. When completion of foaming was confirmed, the reaction solution was concentrated under a reduced pressure and subjected to azeotropic treatment with toluene twice. The thus obtained residue was dissolved in 8.4 ml of dichloromethane and, with cooling on an ice bath, the resulting solution was dropwise added to a solution obtained by dissolving 1.0 g of 5-oxo-2,3,4,5-tetrahydro-1H-1-benzazepine and 1.53 ml of triethylamine in 10 ml of dichloromethane. The reaction solution was warmed up to room temperature and the stirring was continued for 1 hour. The resulting reaction solution was mixed with water and subjected to phase separation to separate dichloromethane layer which was subsequently washed with 0.5N hydrochloric acid and a saturated sodium bicarbonate aqueous solution and dried over anhydrous magnesium sulfate. After removing the solvent by distillation, the thus obtained residue was crystallized from toluene to obtain 1.65 g of 1-(2'-methoxybiphen-4-ylcarbonyl)-5-oxo-2,3,4,5-tetrahydro-1H-1-benzazepine as crude crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05856564
出典データセットuspto-grants-1999_01
ORD IDord-3d58f23de8ca449fac5f0a7037878192
出典メモuspto-grants-1999_01