반응 #3407

ord-94eabea82a724e06b470656c1d0fc4ec

반응 방정식

c1ccc(COc2cncc(C34CCCN3CCC4)c2)cc1
7a-(3-Benzyloxy-5-pyridinyl)-hexahydro-1H-pyrrolizine
Oc1cncc(C23CCCN2CCC3)c1
title compound
수율 63.4%
Oc1cncc(C23CCCN2CCC3)c1
7a-(3-hydroxy-5-pyridinyl)-hexahydro-1H-pyrrolizine
수율 63.4%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The catalyst was removed
  2. 2
    농축the filtrate was concentrated
  3. 3
    기타the residue was chromatographed (silica gel; CHCl3 /MeOH/0.5 % NH4OH, 90:10:0 to 90:10:0.5)

실험 절차

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

DOI: 10.6084/m9.figshare.5104873.v1특허: US05733912uspto-grants-1998_03