(S)-3-Oxiranyl-pyridine → (R)-2-amino-1-(pyridin-3-yl)ethanol
Reaction equation
[O:1]1[CH2:3][C@H:2]1[C:4]1[CH:5]=[N:6][CH:7]=[CH:8][CH:9]=1.CO.[NH4+:12]>>[NH2:12][CH2:3][C@@H:2]([C:4]1[CH:5]=[N:6][CH:7]=[CH:8][CH:9]=1)[OH:1]Participants
3
Procedure
The title compound was prepared from 3-[(2R)-oxiranyl]pyridine (which was obtained in Example 134) and saturated ammonium methanol in substantially the same manner, as described in Example 124. The product was obtained as a brown oil; 1H NMR (300 MHz, DMSO-d6) δ 1.70 (brs, 2H), 2.62-2.74 (m, 2H), 4.46-4.50 (m, 1H), 5.20 (brs, 1H), 7.30-7.34 (m, 1H), 7.68-7.71 (m, 1H), 8.42-8.50 (m, 2H); MS (ES) m/z: 139 (MH+).
Workup
- customThe product was obtained as a brown oil
Sources & evidence
- ORD record
- ord-ebc4da04f4104abc9dab65d4b83f802b
- Source dataset
- uspto-grants-2003_02
- Patent number
- US06525202B2
Reaction notes
Loading…