Potassium Carbonate → HCID 22117339, compound
Reaction equation
[Cl:1][CH2:2][CH2:3][CH2:4][S:5][C:6]1[CH:11]=[CH:10][N:9]=[C:8]([CH2:12][S:13][C:14]2[CH:19]=[CH:18][N:17]=[CH:16][CH:15]=2)[C:7]=1[CH3:20].[Cl:21][C:22]1[S:26][C:25]([CH2:27][N:28]2[CH2:33][CH2:32][NH:31][CH2:30][CH2:29]2)=[CH:24][CH:23]=1.C(=O)([O-])[O-].[K+].[K+]>>[ClH:1].[ClH:21].[ClH:1].[Cl:21][C:22]1[S:26][C:25]([CH2:27][N:28]2[CH2:33][CH2:32][N:31]([CH2:2][CH2:3][CH2:4][S:5][C:6]3[CH:11]=[CH:10][N:9]=[C:8]([CH2:12][S:13][C:14]4[CH:19]=[CH:18][N:17]=[CH:16][CH:15]=4)[C:7]=3[CH3:20])[CH2:30][CH2:29]2)=[CH:24][CH:23]=1Participants
4
Procedure
According to the procedure indicated in Example 7, reaction of 4-(3-chloropropylthio)-3-methyl-2-[(4-pyridinylthio)methyl]pyridine with [1-(5-chlorothiophen-2-yl)methyl]piperazine and potassium carbonate gives, after crystallization from isopropanol/acetone/conc. hydrochloric acid, the title compound; m.p. 160-162° C., dec.; yield 79% of theory.
Workup
- customgives
- customafter crystallization from isopropanol/acetone/conc
Sources & evidence
- ORD record
- ord-4343c5501e6b409b91bb018637b73ae7
- Source dataset
- uspto-grants-2000_12
- Patent number
- US06162809
Reaction notes
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