2-(Methylamino)ethanol → 2-[(2-Hydroxymethyl-pyridin-4-yl)-methyl-amino]-ethanol
Reaction equation
Cl[C:2]1[CH:7]=[CH:6][N:5]=[C:4]([CH2:8][OH:9])[CH:3]=1.[CH3:10][NH:11][CH2:12][CH2:13][OH:14]>>[OH:9][CH2:8][C:4]1[CH:3]=[C:2]([N:11]([CH3:10])[CH2:12][CH2:13][OH:14])[CH:7]=[CH:6][N:5]=1Participants
3
Conditions
- Temperature
- 140 °C
Procedure
A mixture of (4-chloro-pyridin-2-yl)-methanol (20.0 g, 139 mmol) and 2-methylaminoethanol (11.7 ml, 146 mmol) is stirred for 1 h at 140° C. After cooling to room temperature the viscous oil is employed without additional purification for the synthesis described in step b).
Workup
- temperatureAfter cooling to room temperature the viscous oil
- customis employed without additional purification for the synthesis
Sources & evidence
- ORD record
- ord-e858c021fed64fee910963edc0e67db3
- Source dataset
- uspto-grants-2000_03
- Patent number
- US06043242
Reaction notes
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