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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 329727생성일: 2026년 10월 26일

Ethyl chloroformate → 6-chloro-3,4-dihydro-2,4-dimethyl-3-oxo-N-(3-quinuclidinyl)-2H-1,4-benzoxazine-8-carboxamide hydrochloride

https://huagongshe.com/reaction/329727

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl chloroformateHCID 10928—
반응물3-AminoquinuclidineHCID 123238—
반응물Sodium BicarbonateHCID 516892—
반응물6-chloro-3,4-dihydro-2,4-dimethyl-3-oxo-2H-1,4-benzoxazine-8-carboxylic acidHCID 14517234—
용매TetrahydrofuranHCID 8028—
용매TriethylamineHCID 8471—
용매Ethyl AcetateHCID 8857—
생성물6-chloro-3,4-dihydro-2,4-dimethyl-3-oxo-N-(3-quinuclidinyl)-2H-1,4-benzoxazine-8-carboxamide hydrochlorideHCID 19871158—

반응 단계

A solution of 4.28 g of 6-chloro-3,4-dihydro-2,4-dimethyl-3-oxo-2H-1,4-benzoxazine-8-carboxylic acid in 50 ml of tetrahydrofuran is cooled to below 0° C. and 5 ml of triethylamine is added under stirring thereto. Further, 2.0 g of ethyl chlorocarbonate is added and the mixture is stirred for 30 minutes. To the resultant mixture is added 3.0 g of 3-aminoquinuclidine and the mixture stirred for 5 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 ethanolethyl acetate to give 6-chloro-3,4-dihydro-2,4-dimethyl-3-oxo-N-(3-quinuclidinyl)-2H-1,4-benzoxazine-8-carboxamide hydrochloride, melting at 286°-289° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04892872
출처 데이터셋uspto-grants-1990_01
ORD IDord-a25ecd85583747cf86d0793b399b79ea
출처 메모uspto-grants-1990_01