Hydrochloric Acid → HCID 21076988, compound
Reaction equation
[F:1][C:2]([F:40])([F:39])[C:3]1[CH:4]=[C:5]([CH:32]=[C:33]([C:35]([F:38])([F:37])[F:36])[CH:34]=1)[C:6]([N:8]1[CH2:13][CH2:12][N:11]([CH2:14][C:15]#[C:16][C:17]2[CH:18]=[N:19][CH:20]=[CH:21][CH:22]=2)[CH2:10][CH:9]1[CH2:23][C:24]1[CH:29]=[CH:28][C:27]([CH3:30])=[C:26]([OH:31])[CH:25]=1)=[O:7].[ClH:41]>CO.C(OCC)(=O)C>[ClH:41].[ClH:41].[F:39][C:2]([F:1])([F:40])[C:3]1[CH:4]=[C:5]([CH:32]=[C:33]([C:35]([F:36])([F:37])[F:38])[CH:34]=1)[C:6]([N:8]1[CH2:13][CH2:12][N:11]([CH2:14][C:15]#[C:16][C:17]2[CH:18]=[N:19][CH:20]=[CH:21][CH:22]=2)[CH2:10][CH:9]1[CH2:23][C:24]1[CH:29]=[CH:28][C:27]([CH3:30])=[C:26]([OH:31])[CH:25]=1)=[O:7]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of 1-[3,5-bis(trifluoromethyl)benzoyl]-2-(3-hydroxy-4-methylbenzyl)-4-[3-(3-pyridyl)-2-propynyl]-piperazine (0.11 g) in methanol (10 ml) was treated with 4N hydrogen chloride in ethyl acetate (1 ml) and the mixture was evaporated under reduced pressure. The residue was triturated with a mixture of dichloromethane and ethyl acetate and the resulting powder was collected by filtration to give 1-[3,5-bis(trifluoromethyl)benzoyl]-2-(3-hydroxy-4-methylbenzyl)-4-[3-(3-pyridyl)-2-propynyl]piperazine dihydrochloride (0.07 g).
Workup
- customthe mixture was evaporated under reduced pressure
- customThe residue was triturated with a mixture of dichloromethane and ethyl acetate
- filtrationthe resulting powder was collected by filtration
Sources & evidence
- ORD record
- ord-6952d327dc7d4cf9b2dc3e66a7ca0934
- Source dataset
- uspto-grants-2007_01
- Patent number
- US07166598B2
Reaction notes
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