2-[4-(Aminomethyl)phenyl]propan-2-ol → HCID 22612365, compound

HRID 844086Notes

Reaction equation

HRID 844086 reaction equation
[O: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>>[O: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]1

Participants

3

Procedure

Prepared from 2-(Benzooxazol-6-yloxy)-nicotinic acid and 2-(4-aminomethyl-phenyl)-propan-2-ol. mp 92-4° C.

Sources & evidence

ORD record
ord-9bea411909904ff99845d4c64af3d741
Source dataset
uspto-grants-2002_04
Patent number
US06380218B1

Reaction notes

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