2-[4-(Aminomethyl)phenyl]propan-2-ol → HCID 22612288, compound
Reaction equation
[S:1]1[C:5]2[CH:6]=[C:7]([O:10][C:11]3[N:19]=[CH:18][CH:17]=[CH:16][C:12]=3[C:13]([OH:15])=O)[CH:8]=[CH:9][C:4]=2[N:3]=[CH:2]1.[NH2:20][CH2:21][C:22]1[CH:27]=[CH:26][C:25]([C:28]([OH:31])([CH3:30])[CH3:29])=[CH:24][CH:23]=1>>[S:1]1[C:5]2[CH:6]=[C:7]([O:10][C:11]3[N:19]=[CH:18][CH:17]=[CH:16][C:12]=3[C:13]([NH:20][CH2:21][C:22]3[CH:27]=[CH:26][C:25]([C:28]([OH:31])([CH3:29])[CH3:30])=[CH:24][CH:23]=3)=[O:15])[CH:8]=[CH:9][C:4]=2[N:3]=[CH:2]1Participants
3
Procedure
Prepared from 2-(Benzothiazol-6-yloxy)-nicotinic acid and 2-(4-aminomethyl-phenyl)-propan-2-ol. mp195-7° C.
Sources & evidence
- ORD record
- ord-48e7a3dbb34343b5a89830ce5605f2a1
- Source dataset
- uspto-grants-2002_04
- Patent number
- US06380218B1
Reaction notes
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