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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 329725생성일: 2026년 10월 27일

Ethyl chloroformate → 6-chloro-3,4-dihydro-2-methyl-N-(8-methyl-8-azabicyclo[3.2.1]oct-3-yl)-3-oxo-2H-1,4-benzoxazine-8-carboxamide hydrochloride

https://huagongshe.com/reaction/329725

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl chloroformateHCID 10928—
반응물8-Methyl-8-azabicyclo[3.2.1]octan-3-amineHCID 408394—
반응물Sodium BicarbonateHCID 516892—
반응물6-chloro-3,4-dihydro-2-methyl-3-oxo-2H-1,4-benzoxazine-8-carboxylic acidHCID 14517231—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
용매TriethylamineHCID 8471—
용매Ethyl AcetateHCID 8857—
생성물6-chloro-3,4-dihydro-2-methyl-N-(8-methyl-8-azabicyclo[3.2.1]oct-3-yl)-3-oxo-2H-1,4-benzoxazine-8-carboxamide hydrochlorideHCID 19871180—

반응 단계

A solution of 4.8 g of 6-chloro-3,4-dihydro-2-methyl-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 5 ml of triethylamine is added under stirring thereto. Further, 2.5 g of ethyl chlorocarbonate is added and the mixture is stirred at room temperature for 45 minutes. To the resultant mixture is added 3.0 g of 3-amino-8-methyl-8-azabicyclo[3.2.1]octane 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 converted into the corresponding hydrochloride by treating with ethanolic hydrochloric acid followed by recrystallizing from ethanol-water to give 6-chloro-3,4-dihydro-2-methyl-N-(8-methyl-8-azabicyclo[3.2.1]oct-3-yl)-3-oxo-2H-1,4-benzoxazine-8-carboxamide hydrochloride, melting at 325°-328° C. with decomposition.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04892872
출처 데이터셋uspto-grants-1990_01
ORD IDord-32846653c30a4e1d8c2187d6ee8d761c
출처 메모uspto-grants-1990_01