Hydrochloric Acid → N-((1S,2R)-1-(3,5-difluorobenzyl)-3-{[6-ethyl-3,4-dihydro-2H-chromen-4-yl]amino}-2-hydroxypropyl)acetamide
Reaction equation
CC(OC)(C)C.C(Cl)Cl.[F:10][C:11]1[CH:12]=[C:13]([CH:36]=[C:37]([F:39])[CH:38]=1)[CH2:14][C@H:15]([NH:32][C:33](=[O:35])[CH3:34])[C@H:16]([OH:31])[CH2:17][NH:18][C@@H:19]1[C:28]2[C:23](=[CH:24][CH:25]=[C:26]([CH2:29][CH3:30])[CH:27]=2)[O:22][CH2:21][CH2:20]1.Cl>CCOCC.CO>[F:10][C:11]1[CH:12]=[C:13]([CH:36]=[C:37]([F:39])[CH:38]=1)[CH2:14][C@H:15]([NH:32][C:33](=[O:35])[CH3:34])[C@H:16]([OH:31])[CH2:17][NH:18][CH:19]1[C:28]2[C:23](=[CH:24][CH:25]=[C:26]([CH2:29][CH3:30])[CH:27]=2)[O:22][CH2:21][CH2:20]1Participants
7
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
To a MTBE (20 ml), CH2Cl2 (5 ml), MeOH (0.5 ml) solution of N-((1S,2R)-1-(3,5-difluorobenzyl)-3-{[(4S)-6-ethyl-3,4-dihydro-2H-chromen-4-yl]amino}-2-hydroxypropyl)acetamide (0.2 g, 0.5 mmol) was added 1N HCl in Et2O (0.38 ml) and the mixture stirred at room temperature. The final white solid was isolated by removing the solvent and tritration with Et2O. HRMS (ESI+) calcd for C23H28F2N2O3 m/z 419.2146 (M+H)+. Found 419.2166.
Workup
- customThe final white solid was isolated
- customby removing the solvent and tritration with Et2O
Sources & evidence
- ORD record
- ord-7923b44806fa41e1a63879a07c520ffb
- Source dataset
- uspto-grants-2007_07
- Patent number
- US07244725B2
Reaction notes
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