Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triphenyl phosphite → (S)-methyl 6-oxo-6,6a,7,8,9,10-hexahydro-5H-dipyrido[1,2-a:3',2'-e]pyrazine-3-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triphenyl phosphite | HCID 7540 | — |
| 반응물 | (S)-methyl 6-(2-(methoxycarbonyl)piperidin-1-yl)-5-nitronicotinate | HCID 58324510 | — |
| 반응물 | HCID 178418361 | HCID 178418361 | — |
| 촉매 | Platinum | HCID 23939 | — |
| 촉매 | Ammonium metavanadate [UN2859] [Poison] | HCID 62684 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (S)-methyl 6-oxo-6,6a,7,8,9,10-hexahydro-5H-dipyrido[1,2-a:3',2'-e]pyrazine-3-carboxylate | HCID 58324495 | 89% |
반응 단계
In a bomb hydroginator, (S)-methyl 6-(2-(methoxycarbonyl)piperidin-1-yl)-5-nitronicotinate (1.95 g, 6.03 mmol), triphenyl phosphite (0.019 ml, 0.060 mmol), ammonium vanadate (0.056 g, 0.483 mmol) and platinum (5% on carbon, 0.235 g, 0.060 mmol) were mixed in dichloromethane (Volume: 30.2 ml) to give a suspension. The bomb was sealed and pressurized to 110 psi with hydrogen gas. The reaction was stirred at 110 psi 16 h, depressurized, diluted with DCM (100 mL) and refluxed 10 minutes. The hot mixture was filtered through celite and washed with DCM (50 mL). The filtrate was concentrated in vacuo to yield 1.4 g (89%) of the product as a white solid and used without further purification. [M+H] calc'd for C13H15N3O3, 262; found, 262.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08822470B2 |
| 출처 데이터셋 | uspto-grants-2014_09 |
| ORD ID | ord-e5ca4146512848e68549ed74dd7bf83e |
| 출처 메모 | uspto-grants-2014_09 |