Acrylic Acid → N-(4-(2-chloropyrimidin-4-ylthio)phenyl)acrylamide
Reaction equation
ClC1N=C(C2C=CC(SN)=CC=2)C=CN=1.[Cl:16][C:17]1[N:22]=[C:21]([S:23][C:24]2[CH:29]=[CH:28][C:27]([NH2:30])=[CH:26][CH:25]=2)[CH:20]=[CH:19][N:18]=1.[C:31](O)(=[O:34])[CH:32]=[CH2:33]>>[Cl:16][C:17]1[N:22]=[C:21]([S:23][C:24]2[CH:25]=[CH:26][C:27]([NH:30][C:31](=[O:34])[CH:32]=[CH2:33])=[CH:28][CH:29]=2)[CH:20]=[CH:19][N:18]=1Participants
3
Procedure
In a procedure analogous to Example 15, reaction of 4-(2-chloropyrimidin-4-ylthio)benzenamine 2-chloro-4-(4′-aminothiophenyl)pyrimidine (800 mg, 3.37 mmol) and acrylic acid (463 μL, 6.74 mmol) furnished the product (550 mg, 56%).
Sources & evidence
- ORD record
- ord-1395b8747cca4448b5e21b7c656ebec2
- Source dataset
- uspto-grants-2015_05
- Patent number
- US09040549B2
Reaction notes
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