4-Methylcinnamic Acid → HCID 66929289, compound
Reaction equation
[F:1][C:2]([C:5]1[O:9][C:8]([CH2:10][N:11]2[CH:15]=[CH:14][C:13]([NH2:16])=[N:12]2)=[CH:7][CH:6]=1)([F:4])[CH3:3].[C:17]1([CH3:28])[CH:22]=[CH:21][C:20](/[CH:23]=[CH:24]/[C:25](O)=[O:26])=[CH:19][CH:18]=1>>[F:4][C:2]([C:5]1[O:9][C:8]([CH2:10][N:11]2[CH:15]=[CH:14][C:13]([NH:16][C:25](=[O:26])/[CH:24]=[CH:23]/[C:20]3[CH:21]=[CH:22][C:17]([CH3:28])=[CH:18][CH:19]=3)=[N:12]2)=[CH:7][CH:6]=1)([F:1])[CH3:3]Participants
3
Procedure
Following general procedure B, starting from 1-[5-(1,1-difluoro-ethyl)-furan-2-ylmethyl]-1H-pyrazol-3-ylamine and (E)-3-p-tolyl-acrylic acid. LC-MS-conditions 05b: tR=1.12 min; [M+H]+=372.16.
Sources & evidence
- ORD record
- ord-3a23629b3ace4d358f766b0e3b17028e
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08288419B2
Reaction notes
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