3-[(2S)-oxiran-2-yl]pyridine → (S)-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-[(2S)-oxiranyl]pyridine (which was obtained in Example 129) and saturated ammonium methanol in substantially the same manner, as described in Example 124. The product was obtained as a brown oil; 1H NMR (400 MHz, DMSO-d6) δ 1.60 (brs, 2 H), 2.59–2.71 (m, 2 H), 4.47–4.50 (m, 1 H), 5.20 (brs, 1 H), 7.31–7.34 (m, 1 H), 7.68–7.71 (m, 1 H), 8.42–8.43 (m, 1 H), 8.50–8.51 (m, 1 H); MS (ES) m/z: 139 (MH+).
Workup
- customThe product was obtained as a brown oil
Sources & evidence
- ORD record
- ord-cf33eec1fd874d97a738ecb769d72049
- Source dataset
- uspto-grants-2006_04
- Patent number
- US07022716B2
Reaction notes
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