6-Chloropyrazin-2-ylthiourea → (6-Chloro-pyrazin-2-yl)-[5-(4-methanesulfonyl-3-trifluoromethyl-phenyl)-4-methyl-thiazol-2-yl]-amine
Reaction equation
[CH3:1][S:2]([C:5]1[CH:10]=[CH:9][C:8]([CH2:11][C:12](=O)[CH3:13])=[CH:7][C:6]=1[C:15]([F:18])([F:17])[F:16])(=[O:4])=[O:3].[Cl:19][C:20]1[N:25]=[C:24]([NH:26][C:27]([NH2:29])=[S:28])[CH:23]=[N:22][CH:21]=1>>[Cl:19][C:20]1[N:25]=[C:24]([NH:26][C:27]2[S:28][C:11]([C:8]3[CH:9]=[CH:10][C:5]([S:2]([CH3:1])(=[O:4])=[O:3])=[C:6]([C:15]([F:18])([F:17])[F:16])[CH:7]=3)=[C:12]([CH3:13])[N:29]=2)[CH:23]=[N:22][CH:21]=1Participants
3
Procedure
The titled compound is prepared from 1-(4-methanesulfonyl-3-trifluoromethyl-phenyl) propan-2-one (59c) and 6-chloro-pyrazin-2-yl-thiourea.
Sources & evidence
- ORD record
- ord-de2ec74ff78648d1a0c0c4744b09383a
- Source dataset
- uspto-grants-2011_09
- Patent number
- US08017608B2
Reaction notes
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