Hydrochloric Acid → HCID 131716676, compound
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH2:13][CH2:12][N:11]([CH2:14][C:15]([N:17]3[CH2:22][CH:21]=[C:20]([C:23]4[CH:28]=[CH:27][CH:26]=[C:25]([C:29]([F:32])([F:31])[F:30])[CH:24]=4)[N:19]4[N:33]=[CH:34][C:35]([C:36]#[N:37])=[C:18]34)=[O:16])[CH2:10][CH2:9]2)=[CH:4][CH:3]=1.[ClH:38].CCOCC>C(OCC)(=O)C>[ClH:38].[F:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[CH2:13][CH2:12][N:11]([CH2:14][C:15]([N:17]3[CH2:22][CH:21]=[C:20]([C:23]4[CH:28]=[CH:27][CH:26]=[C:25]([C:29]([F:31])([F:30])[F:32])[CH:24]=4)[N:19]4[N:33]=[CH:34][C:35]([C:36]#[N:37])=[C:18]34)=[O:16])[CH2:10][CH2:9]2)=[CH:6][CH:7]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A 6.6 g portion of 4-[[4-(4-fluorophenyl)-1-piperazinyl]acetyl]-4,5-dihydro-7-[3-(trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carbonitrile was heated to solution in 100 ml of ethyl acetate, then cooled and acidified with 25 ml of 2.44N ethanolic hydrochloric acid. Ether was added, the solid collected, heated to boiling in 500 ml of ethanol, then cooled and the crystalline salt collected, giving 5.7 g of the desired product, mp 242°-244° C.
Workup
- temperaturecooled
- customthe solid collected
- temperatureheated
- temperaturecooled
- customthe crystalline salt collected
Sources & evidence
- ORD record
- ord-35cbf1c6a5384f19a37d3f2956d3e59f
- Source dataset
- uspto-grants-1990_10
- Patent number
- US04963553
Reaction notes
Loading…