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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1073587생성일: 2026년 10월 25일

Hydrazinecarboxaldehyde, 1-methyl- → 8-chloro-3-ethoxycarbonyl-7-fluoro-1-(N-formyl-N-methylamino)-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridine

https://huagongshe.com/reaction/1073587

반응식

참여 물질

역할이름HCID투입량
반응물Hydrazinecarboxaldehyde, 1-methyl-HCID 12962—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물Ethyl 2-(2,7-dichloro-6-fluoroquinoline-3-carbonyl)-3-dimethylaminoacrylateHCID 54015905—
용매EthanolHCID 702—
생성물8-chloro-3-ethoxycarbonyl-7-fluoro-1-(N-formyl-N-methylamino)-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridineHCID 1470055186.9%

반응 단계

The 8-chloro-3-ethoxycarbonyl-7-fluoro-1-(N-formyl-N-methylamino)-4-oxo-1,4-dihydrobenzo [b][1,8]naphthyridine is prepared under the conditions described in Example 1 but starting from 19.25 g of ethyl 2-(2,7-dichloro-6-fluoroquinoline-3-carbonyl)-3-dimethylaminoacrylate, 4.05 g of N-formyl-N-methylhydrazine and 1.6 g of DBU in 200 cm3 of ethanol. 16.4 g of 8-chloro-3-ethoxycarbonyl-7-fluoro-1-(N-formyl-N-methylamino)-4-oxo-1,4-dihy drobenzo [b][1,8]naphthyridine are obtained in the form of a colourless solid melting at 296°-298° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04970213
출처 데이터셋uspto-grants-1990_11
ORD IDord-2f6f9702c2b5461ab276fb74b7638975
출처 메모uspto-grants-1990_11