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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 622483생성일: 2026년 10월 25일

Acetonitrile → 10-[3-(aminomethyl)-1-pyrrolidinyl]-9-fluoro-2,3-dihydro-methyl-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acid

https://huagongshe.com/reaction/622483

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물8,9-Difluoro-3-methyl-6-oxo-2,3-dihydro-6H-1-oxa-3a-aza-phenalene-5-carboxylic acidHCID 534278—
반응물3-PyrrolidinemethanamineHCID 5068775—
생성물10-[3-(aminomethyl)-1-pyrrolidinyl]-9-fluoro-2,3-dihydro-methyl-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acidHCID 70418225—

반응 단계

0.75 g (0.27 mmole) of 9,10-difluoro-2,3-dihydro3-methyl-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acid, 40 ml acetonitrile, and 0.80 g (8.0 mmole) of 3-pyrrolidinemethanamine were refluxed overnight. The solvent was removed at reduced pressure and the residue titurated with 40 ml of ethanol/ether (1:1), to give 0.90 g of 10-[3-(aminomethyl)-1-pyrrolidinyl]-9-fluoro-2,3-dihydro- methyl-7-oxo-7H-pyrido[1,2,3-de]-1,4-benzoxazine-6-carboxylic acid, mp 213°-216° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04771054
출처 데이터셋uspto-grants-1988_09
ORD IDord-23b85bad7c614b4d9fbedc7ee3c99edd
출처 메모uspto-grants-1988_09