Hydrochloric Acid → HCID 23658600, compound
Reaction equation
[F:1][C:2]([F:35])([F:34])[C:3]1[CH:33]=[CH:32][C:6]([O:7][CH:8]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[CH2:9][CH2:10][N:11]([CH3:25])[C:12]([CH2:14][CH2:15][CH2:16][NH:17]C(=O)OC(C)(C)C)=[O:13])=[CH:5][CH:4]=1.[ClH:36]>CCOC(C)=O>[ClH:36].[F:1][C:2]([F:34])([F:35])[C:3]1[CH:4]=[CH:5][C:6]([O:7][CH:8]([C:26]2[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=2)[CH2:9][CH2:10][N:11]([CH3:25])[C:12](=[O:13])[CH2:14][CH2:15][CH2:16][NH2:17])=[CH:32][CH:33]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
tert-Butyl 3-(N-(3-(4-(Trifluoromethyl)phenoxy)-3-phenylpropyl)-N-methyl carbamoyl)propylcarbamate (AN-229) was prepared as described in WO 2005/092392. AN-229 (0.5 mmol) was added to a solution of HCl in EtOAc (35 ml) and the resulting mixture was stirred for 3 hours. The solvent was thereafter evaporated and the product, AN-227, was obtained in quantitative yield.
Workup
- customThe solvent was thereafter evaporated
- customthe product, AN-227, was obtained in quantitative yield
Sources & evidence
- ORD record
- ord-1d46d8150deb45278889c8e0f3895343
- Source dataset
- uspto-grants-2013_02
- Patent number
- US08377990B2
Reaction notes
Loading…