1-Isopropylpiperazine → 4-(2-(4-Isopropylpiperazin-1-yl)-pyrimidin-5-yl)-benzonitrile dihydrochloride
Reaction equation
[Cl:1][C:2]1[N:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][C:11]([C:14]#[N:15])=[CH:10][CH:9]=2)=[CH:4][N:3]=1.[CH:16]([N:19]1[CH2:24][CH2:23][NH:22][CH2:21][CH2:20]1)([CH3:18])[CH3:17]>>[ClH:1].[ClH:1].[CH:16]([N:19]1[CH2:24][CH2:23][N:22]([C:2]2[N:7]=[CH:6][C:5]([C:8]3[CH:13]=[CH:12][C:11]([C:14]#[N:15])=[CH:10][CH:9]=3)=[CH:4][N:3]=2)[CH2:21][CH2:20]1)([CH3:18])[CH3:17]Participants
3
Procedure
The title compound was prepared by a similar procedure to that described in Example 1, starting from 2-chloro-5-(4-cyanophenyl)pyrimidine and 1-isopropylpiperazine.
Sources & evidence
- ORD record
- ord-987441edfe2e44d28981ee9fb51dd119
- Source dataset
- uspto-grants-2014_09
- Patent number
- US08846677B2
Reaction notes
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