Hydrochloric Acid → HCID 15057040, compound
Reaction equation
C([NH:4][CH2:5][CH2:6][C:7]1[CH:12]=[CH:11][C:10]([CH:13]([C:21]2[CH:22]=[N:23][CH:24]=[CH:25][CH:26]=2)[CH2:14][CH2:15][CH2:16][CH2:17][C:18]([OH:20])=[O:19])=[CH:9][CH:8]=1)(=O)C.Cl>>[NH2:4][CH2:5][CH2:6][C:7]1[CH:8]=[CH:9][C:10]([CH:13]([C:21]2[CH:22]=[N:23][CH:24]=[CH:25][CH:26]=2)[CH2:14][CH2:15][CH2:16][CH2:17][C:18]([OH:20])=[O:19])=[CH:11][CH:12]=1Participants
3
Procedure
4.0 g of 6-(4-(2-acetylaminoethyl)phenyl)-6-(3-pyridyl)hexanoic acid are refluxed for 18 hours with 50 ml of half concentrated hydrochloric acid. The mixture is then rotary evaporated and the residue is purified by chromatography over a column of silica gel using methanol.
Workup
- customThe mixture is then rotary evaporated
- customthe residue is purified by chromatography over a column of silica gel
Sources & evidence
- ORD record
- ord-8567222ed63846d8a5ee0d437b647a12
- Source dataset
- uspto-grants-1994_03
- Patent number
- US05294626
Reaction notes
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