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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 580592생성일: 2026년 10월 25일

8,9-Difluoro-3-methyl-6-oxo-2,3-dihydro-6H-1-oxa-3a-aza-phenalene-5-carboxylic acid → 10-(cis-3-t-Butoxycarbonylamino-4-methyl-1-pyrrolidinyl)-9-fluoro-2,3-dihydro-3-methyl-7-oxo-7H-pyrido[1,2,3-de][1,4]benzoxazine-6-carboxylic acid

https://huagongshe.com/reaction/580592

반응식

참여 물질

역할이름HCID투입량
반응물8,9-Difluoro-3-methyl-6-oxo-2,3-dihydro-6H-1-oxa-3a-aza-phenalene-5-carboxylic acidHCID 534278—
반응물(3S,4S)-3-(Boc-amino)-4-methylpyrrolidineHCID 11138119—
용매Dimethyl SulfoxideHCID 679—
생성물10-(cis-3-t-Butoxycarbonylamino-4-methyl-1-pyrrolidinyl)-9-fluoro-2,3-dihydro-3-methyl-7-oxo-7H-pyrido[1,2,3-de][1,4]benzoxazine-6-carboxylic acidHCID 7041939770.7%

반응 단계

A mixture of 9,10-difluoro-2,3-dihydro-3-methyl-7-oxo-7H-pyrido[1,2,3-de][1,4]benzoxazine-6-carboxylic acid (0.5 g), anhydrous dimethyl sulfoxide (10 ml) and cis-3-t-butoxycarbonylamino-4-methylpyrrolidine (0.54 g) was stirred for 2 hours at 90°-100° C. and then concentrated. To the residue was added methanol and the resulting precipitate was collected by filtration and then washed with cold methanol to give the title compound (0.58 g) as yellowish powder, mp 219°-220° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04753953
출처 데이터셋uspto-grants-1988_06
ORD IDord-b7f2201273df4e4fa8288ce078d6c38d
출처 메모uspto-grants-1988_06