Methanol → Methyl 6-(4-(2-aminoethyl)phenyl)-6-(3-pyridyl)hex-5-enoate
Reaction equation
C([NH:4][CH2:5][CH2:6][C:7]1[CH:12]=[CH:11][C:10]([C:13]([C:21]2[CH:22]=[N:23][CH:24]=[CH:25][CH:26]=2)=[CH:14][CH2:15][CH2:16][CH2:17][C:18]([OH:20])=[O:19])=[CH:9][CH:8]=1)(=O)C.[CH3:27]O>>[NH2:4][CH2:5][CH2:6][C:7]1[CH:12]=[CH:11][C:10]([C:13]([C:21]2[CH:22]=[N:23][CH:24]=[CH:25][CH:26]=2)=[CH:14][CH2:15][CH2:16][CH2:17][C:18]([O:20][CH3:27])=[O:19])=[CH:9][CH:8]=1Participants
3
Procedure
Prepared by hydrolysis of 6-(4-(2-acetylaminoethyl)-phenyl)-6-(3-pyridyl)hex-5-enoic acid and subsequent esterification with methanol analogously to Example 8b.
Sources & evidence
- ORD record
- ord-56070f633c464eaa985ccdb7488c56ee
- Source dataset
- uspto-grants-1995_06
- Patent number
- US05426119
Reaction notes
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