Hydantoin → HCID 68660069, compound
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[CH:13]=[CH:12][N:11]2[N:14]=[CH:15][C:16]([CH:17]=[C:18]3S[C:21](=[O:23])[NH:20][C:19]3=[O:24])=[C:10]2[N:9]=1.[NH:25]1CC(=O)NC1=O>>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[CH:13]=[CH:12][N:11]2[N:14]=[CH:15][C:16]([CH:17]=[C:18]3[NH:25][C:21](=[O:23])[NH:20][C:19]3=[O:24])=[C:10]2[N:9]=1Participants
3
Procedure
5-((5-(2-fluorophenyl)pyrazolo[1,5-a]pyrimidin-3-yl)methylene)imidazolidine-2,4-dione was prepared using the same procedure as for the synthesis of 5-((5-(2-fluorophenyl)pyrazolo[1,5-a]pyrimidin-3-yl)methylene)thiazolidine-2,4-dione using hydantoin instead of thiazolidine-2,4-dione.
Sources & evidence
- ORD record
- ord-304f7f7763874313b0dbbc1a50b3120a
- Source dataset
- uspto-grants-2013_02
- Patent number
- US08367681B2
Reaction notes
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