Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 69606생성일: 2026년 10월 24일
Triphenyl phosphite → (S)-methyl 4-isopropyl-3-methyl-2-oxo-1,2,3,4-tetrahydropyrido[3,2-b]pyrazine-7-carboxylate
https://huagongshe.com/ko/reaction/69606
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triphenyl phosphite | HCID 7540 | — |
| 반응물 | (S)-methyl 6-((1-ethoxy-1-oxopropan-2-yl)(isopropyl)amino)-5-nitronicotinate | HCID 58324420 | — |
| 촉매 | Platinum | HCID 23939 | — |
| 촉매 | Ammonium metavanadate | HCID 516859 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (S)-methyl 4-isopropyl-3-methyl-2-oxo-1,2,3,4-tetrahydropyrido[3,2-b]pyrazine-7-carboxylate | HCID 59416799 | 94.3% |
반응 단계
(S)-methyl 6-((1-ethoxy-1-oxopropan-2-yl)(isopropyl)amino)-5-nitronicotinate (0.900 g, 2.65 mmol) was dissolved in dichloromethane (10 mL). To this solution was added triphenyl phosphite (3.0 mg, 9.7 umol), ammonium metavanadate (30 mg, 0.265 mmol) and Pt/C (5% wt., 0.120 g). The reaction mixture was hydrogenated at 80 psi at 25° C. for 6 h. The mixture was filtered through a small pad of celite and the pad was washed with dichloromethane (20 mL). The combined filtrates were concentrated in vacuo and crystallized with ethyl ether to afford the title compounds as a white solid (0.658 g, 94%). 1H NMR (400 MHz, CHLOROFORM-d) δ (ppm): 1.33 (d, J=6.82 Hz, 3 H) 1.36-1.41 (m, 6 H) 3.90 (s, 3 H) 4.34 (q, J=6.65 Hz, 1 H) 4.86 (m, 1 H) 7.52 (d, J=1.77 Hz, 1 H) 8.59 (d, J=1.77 Hz, 1 H) 8.73 (br. s., 1 H); [M+H] calc'd for C13H17N3O3, 264; found, 264.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08822470B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-54c36d5df05246269b0dc9e22713aeea |
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| 출처 메모 | uspto-grants-2014_09 |
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