Potassium Carbonate → 4-[[4-[(2,6-Dichlorophenyl)methyl]-1-piperazinyl]acetyl]-4.5-dihydro-6-methyl-7-[3-(trifluoromethyl)phenyl]pyrazolo[1,5-a]pyrimidine-3-carbonitrile, hydrochloride
Reaction equation
[Cl:1][CH2:2][C:3]([N:5]1[CH2:10][C:9]([CH3:11])=[C:8]([C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([C:18]([F:21])([F:20])[F:19])[CH:13]=2)[N:7]2[N:22]=[CH:23][C:24]([C:25]#[N:26])=[C:6]12)=[O:4].[Cl:27][C:28]1[CH:40]=[CH:39][CH:38]=[C:37]([Cl:41])[C:29]=1[CH2:30][N:31]1[CH2:36][CH2:35][NH:34][CH2:33][CH2:32]1.C(=O)([O-])[O-].[K+].[K+]>C1(C)C=CC=CC=1>[ClH:1].[Cl:41][C:37]1[CH:38]=[CH:39][CH:40]=[C:28]([Cl:27])[C:29]=1[CH2:30][N:31]1[CH2:32][CH2:33][N:34]([CH2:2][C:3]([N:5]2[CH2:10][C:9]([CH3:11])=[C:8]([C:12]3[CH:17]=[CH:16][CH:15]=[C:14]([C:18]([F:20])([F:19])[F:21])[CH:13]=3)[N:7]3[N:22]=[CH:23][C:24]([C:25]#[N:26])=[C:6]23)=[O:4])[CH2:35][CH2:36]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 1 g of 4-(chloroacetyl)-7-[3-(trifluoromethyl)phenyl]-4,5-dihydro-6-methylpyrazolo[1,5-a]pyrimidine-3-carbonitrile, 1 g of 2,6-dichlorobenzylpiperazine, 600 mg of potassium carbonate and 100 ml of toluene was reacted as described in Example 16, giving the base form of the product, which was converted to the hydrochloride salt by the procedure of Example 97, giving 1.66 g, mp 252°-254° C.
Workup
- customwas reacted
- customgiving the base form of the product, which
- customgiving 1.66 g, mp 252°-254° C.
Sources & evidence
- ORD record
- ord-fd34d52b5bc544f9bdacaed8d1e78b1b
- Source dataset
- uspto-grants-1990_10
- Patent number
- US04963553
Reaction notes
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