Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methylamine → Ethyl 4-hydroxy-1-methyl-2-oxo-7-(trifluoromethyl)-1,2-dihydro-1,8-naphthyridine-3-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methylamine | HCID 6329 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Methyl 2-chloro-6-(trifluoromethyl)pyridine-3-carboxylate | HCID 46311111 | — |
| 반응물 | Methyl 2-(methylamino)-6-(trifluoromethyl)nicotinate | HCID 57671595 | — |
| 생성물 | Ethyl 4-hydroxy-1-methyl-2-oxo-7-(trifluoromethyl)-1,2-dihydro-1,8-naphthyridine-3-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08048894B2 |
| 출처 데이터셋 | uspto-grants-2011_11 |
| ORD ID | ord-7adee1f28d6d49f8b98e7e12b4a05b75 |
| 출처 메모 | uspto-grants-2011_11 |