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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 329730생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/329730

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Ethyl chloroformateHCID 10928—
반응물1-Benzylpiperidin-3-amineHCID 421694—
반응물Sodium BicarbonateHCID 516892—
반응물6-Chloro-3-oxo-3,4-dihydro-2H-1,4-benzoxazine-8-carboxylic acidHCID 14719836—
용매TetrahydrofuranHCID 8028—
용매TriethylamineHCID 8471—
용매Ethyl AcetateHCID 8857—
생성물N-(1-benzyl-4-piperidyl)-6-chloro-3,4-dihydro-3-oxo-2H-1,4-benzoxazine-8-carboxamideHCID 14719844—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04892872
출처 데이터셋uspto-grants-1990_01
ORD IDord-e603d9f08ec24ad28c6d4507c3b1bd4b
출처 메모uspto-grants-1990_01