Hydrochloric Acid → 3-((trans-1,5-dimethyl-2-(S)-pyrrolidinyl)methoxy)pyridine dihydrochloride
Reaction equation
[CH3:1][N:2]1[CH:6]([CH3:7])[CH2:5][CH2:4][C@H:3]1[CH2:8][O:9][C:10]1[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=1.[ClH:16]>CCOCC>[ClH:16].[ClH:16].[CH3:1][N:2]1[C@H:6]([CH3:7])[CH2:5][CH2:4][C@H:3]1[CH2:8][O:9][C:10]1[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A 25 mg sample of the compound of compound from step 89a was treated with HCl in ether according to Example 14c to afford 37 mg of the title compound. MS (DCI/NH3) m/e: 207 (M+H)+. 1H NMR (D2O, 300 MHz) δ: 8.42-8.38 (m, 1H), 8.34-8.28 (m, 11), 7.80-7.76 (m, 1H1), 7.67-7.63 (m, 1H), 4.60-4.54 (m, 11H), 4.47-4.41 (m, 1H), 4.03-3.95 (m, 1H), 3.62-3.52 (m, 1H), 3.03 (s, 3H), 2.40-2.30 (m, 2H), 2.13-2.03 (m, 1H1), 1.93-1.80 (m, 1H), 1.47 (d, J=6.7 Hz, 3H). [α]25D =+15.420 (c=0.50, methanol). Anal. Calc. for C12H18N2O·0.40 HCl: C, 49.06; H, 7.00; N, 9.54; Found: C, 49.22; H, 6.47; N, 9.69.