1-Methylpiperazine → 2-(2-Hydroxyphenyl)-1-(4-methylpiperazino)-1-ethanone
Reaction equation
[CH3:1][N:2]1[CH2:7][CH2:6][NH:5][CH2:4][CH2:3]1.[O:8]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH2:10][C:9]1=[O:17]>>[OH:8][C:16]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[CH2:10][C:9]([N:5]1[CH2:6][CH2:7][N:2]([CH3:1])[CH2:3][CH2:4]1)=[O:17]Participants
3
Conditions
- Temperature
- 85 °C
Procedure
N-Methylpiperazine (1.52 g) was added to 2-coumaranone (2.01 g) and stirred for 3.5 hours at 85° C., thereby yielding the entitled compound (3.57 g) as pale brown solid.
Sources & evidence
- ORD record
- ord-7ba78af36f1645d381e9675a77a3bd69
- Source dataset
- uspto-grants-2002_01
- Patent number
- US06339154B1
Reaction notes
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