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HRID 329730作成日:2026年10月27日

Dimethylformamide → N-(1-benzyl-4-piperidyl)-6-chloro-3,4-dihydro-3-oxo-2H-1,4-benzoxazine-8-carboxamide

https://huagongshe.com/reaction/329730

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Ethyl chloroformateHCID 10928—
反応物1-Benzylpiperidin-3-amineHCID 421694—
反応物Sodium BicarbonateHCID 516892—
反応物6-Chloro-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-8-carboxylic acidHCID 14719836—
溶媒TetrahydrofuranHCID 8028—
溶媒TriethylamineHCID 8471—
溶媒Ethyl AcetateHCID 8857—
生成物N-(1-benzyl-4-piperidyl)-6-chloro-3,4-dihydro-3-oxo-2H-1,4-benzoxazine-8-carboxamideHCID 14719844—

反応手順

A solution of 4.5 g of 6-chloro-3,4-dihydro-3-oxo-2H-1,4-benzoxazine-8-carboxylic acid in 100 ml of tetrahydrofuran and 10 ml of dimethylformamide is cooled to below 0° C. and 2.5 ml of triethylamine is added under stirring thereto. Further, 2.4 g of ethyl chlorocarbonate is added and the mixture is stirred while keeping below 50° C. for an hour. To the resultant mixture is added 3.6 g of 3-amino-1benzylpiperidine and the mixture stirred for 4 hours. After completion of the reaction, aqueous sodium hydrogen carbonate and ethyl acetate are added. The organic layer is separated, washed with water and dried over magnesium sulfate. The solvent is distilled off and the residue is recrystallized from ethanol-ethyl acetate to give N-(1-benzyl-4-piperidyl) -6-chloro-3,4-dihydro-3-oxo-2H-1,4-benzoxazine-8-carboxamide, melting at 203°-206° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04892872
出典データセットuspto-grants-1990_01
ORD IDord-e603d9f08ec24ad28c6d4507c3b1bd4b
出典メモuspto-grants-1990_01