돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 553542생성일: 2026년 10월 25일

Methylamine → Ethyl 4-hydroxy-1-methyl-2-oxo-7-(trifluoromethyl)-1,2-dihydro-1,8-naphthyridine-3-carboxylate

https://huagongshe.com/reaction/553542

반응식

참여 물질

역할이름HCID투입량
반응물MethylamineHCID 6329—
반응물TetrahydrofuranHCID 8028—
반응물Potassium CarbonateHCID 11430—
반응물Methyl 2-chloro-6-(trifluoromethyl)pyridine-3-carboxylateHCID 46311111—
반응물Methyl 2-(methylamino)-6-(trifluoromethyl)nicotinateHCID 57671595—
생성물Ethyl 4-hydroxy-1-methyl-2-oxo-7-(trifluoromethyl)-1,2-dihydro-1,8-naphthyridine-3-carboxylateHCID 57671568—

반응 단계

Methyl 2-(methylamino)-6-(trifluoromethyl)nicotinate. A mixture of methyl 2-chloro-6-(trifluoromethyl)nicotinate (3.82 g) and K2CO3 (5.6 g, 40 mmol) in THF (25 mL) was stirred under nitrogen for 15 minutes. To the mixture was added a 2M solution of methylamine in THF (10 mL, 20 mmol) and stirring was continued for 63 hours. The reaction mixture was filtered over Celite®, and the filtrate was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (DCM) to give the title compound. MS (ESI, pos. ion) m/z: 235 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08048894B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-7adee1f28d6d49f8b98e7e12b4a05b75
출처 메모uspto-grants-2011_11