Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
7a-(3-benzyloxy-5-pyridinyl)-hexahydro-1H-pyrrolizine → 7a-(3-hydroxy-5-pyridinyl)-hexahydro-1H-pyrrolizine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 7a-(3-benzyloxy-5-pyridinyl)-hexahydro-1H-pyrrolizine | HCID 18934754 | — |
| 촉매 | Platinum | HCID 23939 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 7a-(3-hydroxy-5-pyridinyl)-hexahydro-1H-pyrrolizine | HCID 18934730 | 63.4% |
반응 단계
7a-(3-Benzyloxy-5-pyridinyl)-hexahydro-1H-pyrrolizine (260 mg, 0.88 mmol, from step 16b) was dissolved in methanol (9 mL), 10% Pt/C (35 mg) was added, and the mixture stirred under 1 arm of H2 for 16 hours. The catalyst was removed, the filtrate was concentrated, and the residue was chromatographed (silica gel; CHCl3 /MeOH/0.5 % NH4OH, 90:10:0 to 90:10:0.5) to afford the title compound as a white solid (114 mg, 63%). 1H NMR D2O, 300 MHz) δ2.07-2.40 (m, 6H), 2.49-2.58 (m, 2H), 3.26-3.34 (m, 2H), 3.71-3.80 (m, 2H), 7.00 (dd, J=2.4, 2.0 Hz, 1H), 7.80 (d, J=2.0 Hz, 1H), 7.85 (d, J=2.4 Hz, 1H): MS (CI/NH3) m/z: 205 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05733912 |
| 출처 데이터셋 | uspto-grants-1998_03 |
| ORD ID | ord-94eabea82a724e06b470656c1d0fc4ec |
| 출처 메모 | uspto-grants-1998_03 |