Hydrochloric Acid → HCID 86584236, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:31]=[CH:32][C:33]=1[Cl:34])[CH2:5][C@@H:6]1[CH2:11][N:10]([CH2:12][CH2:13][OH:14])[CH2:9][CH2:8][N:7]1[C:15](=[O:30])[C:16]1[CH:21]=[C:20]([C:22]([F:25])([F:24])[F:23])[CH:19]=[C:18]([C:26]([F:29])([F:28])[F:27])[CH:17]=1.Cl>C(OCC)(=O)C>[ClH:1].[Cl:1][C:2]1[CH:3]=[C:4]([CH:31]=[CH:32][C:33]=1[Cl:34])[CH2:5][C@@H:6]1[CH2:11][N:10]([CH2:12][CH2:13][OH:14])[CH2:9][CH2:8][N:7]1[C:15](=[O:30])[C:16]1[CH:17]=[C:18]([C:26]([F:28])([F:27])[F:29])[CH:19]=[C:20]([C:22]([F:25])([F:24])[F:23])[CH:21]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of (2R)-2-(3,4-dichlorobenzyl)-1-[3,5-bis(trifluoromethyl)benzoyl]-4-(2-hydroxyethyl)piperazine (50 mg) in ethyl acetate (3 ml) was treated with 4N hydrogen chloride in ethyl acetate solution (0.2 ml) and the resulting mixture was concentrated in vacuo to give (2R)-2-(3,4-dichlorobenzyl)-1-[3,5-bis(trifluoromethyl)benzoyl]-4-(2-hydroxyethyl)piperazine hydrochloride (45 mg) as a powder.
Workup
- concentrationthe resulting mixture was concentrated in vacuo
Sources & evidence
- ORD record
- ord-be6cc6b9b63e4b45ba6516140e472fc2
- Source dataset
- uspto-grants-2000_07
- Patent number
- US06087357
Reaction notes
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