돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3311생성일: 2026년 10월 23일

7a-(3-benzyloxy-5-pyridinyl)-hexahydro-1H-pyrrolizine → 7a-(3-hydroxy-5-pyridinyl)-hexahydro-1H-pyrrolizine

https://huagongshe.com/ko/reaction/3311

반응식

참여 물질

역할이름HCID투입량
반응물7a-(3-benzyloxy-5-pyridinyl)-hexahydro-1H-pyrrolizineHCID 18934754—
촉매PlatinumHCID 23939—
용매MethanolHCID 887—
생성물7a-(3-hydroxy-5-pyridinyl)-hexahydro-1H-pyrrolizineHCID 1893473063.4%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05733912
출처 데이터셋uspto-grants-1998_03
ORD IDord-94eabea82a724e06b470656c1d0fc4ec
출처 메모uspto-grants-1998_03