Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triphenyl phosphite → Methyl 4-benzyl-2-oxo-1,2,3,4-tetrahydropyrido[2,3-b]pyrazine-7-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triphenyl phosphite | HCID 7540 | — |
| 반응물 | Methyl 6-(benzyl(2-ethoxy-2-oxoethyl)amino)-5-nitronicotinate | HCID 59416801 | — |
| 반응물 | HCID 178418361 | HCID 178418361 | — |
| 촉매 | Platinum | HCID 23939 | — |
| 촉매 | Ammonium metavanadate | HCID 516859 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Methyl 4-benzyl-2-oxo-1,2,3,4-tetrahydropyrido[2,3-b]pyrazine-7-carboxylate | HCID 58324373 | 71% |
반응 단계
Methyl 6-(benzyl(2-ethoxy-2-oxoethyl)amino)-5-nitronicotinate (445 mg g, 1.19 mmol) was dissolved in dichloromethane (5 mL). To the yellow solution was added ammonium metavanadate (10.0 mg, 0.085 mmol), triphenyl phosphite (aprox 10 ul, 0.032 mmol), and Pt/C (50 mg, 5% w/w). The reaction mixture was pressurized with hydrogen gas (75 psi) and stirred at room temperature for 48 h. The reaction was then depressurized and diluted with dichloromethane (20 mL) which was then refluxed for 30 min. The hot solution was filtered through a pad of celite and washed with hot dichloromethane (3×10 mL). The filtrate was concentrated to yield the title compound (250 mg, 71%) as a white solid. [M+H] calc'd for C16H15N3O3, 298; found, 298.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08822470B2 |
| 출처 데이터셋 | uspto-grants-2014_09 |
| ORD ID | ord-a6c2a1d20e874012b3a7f0e995912085 |
| 출처 메모 | uspto-grants-2014_09 |