4-(Morpholinomethyl)aniline → 4-(Pyridin-2-ylmethoxy)aniline
Reaction equation
N1(CC2C=CC(N)=CC=2)CCOCC1.[N+:15]([C:18]1[CH:31]=[CH:30][C:21]([O:22][CH2:23][C:24]2[CH:29]=[CH:28][CH:27]=[CH:26][N:25]=2)=[CH:20][CH:19]=1)([O-])=O>>[N:25]1[CH:26]=[CH:27][CH:28]=[CH:29][C:24]=1[CH2:23][O:22][C:21]1[CH:30]=[CH:31][C:18]([NH2:15])=[CH:19][CH:20]=1Participants
3
Procedure
Using the procedure described for the preparation of 4-Morpholin-4-ylmethyl-phenylamine, 1.16 g (100%) of white crystals is obtained from 1.5 g (5.55 mmol) of ′2-[(4-nitrophenoxy)methyl]pyridine; mp 50-51° C. MS (ESI) m/z 201.1 (M+1)+.
Sources & evidence
- ORD record
- ord-b2a3fbfb990b44a88fbb7659b5f206c1
- Source dataset
- uspto-grants-2010_05
- Patent number
- US07713994B2
Reaction notes
Loading…