3-(furan-2-yl)-1H-pyrazol-5-amine → HCID 67112676, compound
Reaction equation
[NH2:1][C:2]1[CH:6]=[C:5]([C:7]2[O:8][CH:9]=[CH:10][CH:11]=2)[NH:4][N:3]=1.[C:12]1([C:21]2[CH:26]=[CH:25][C:24]([C:27]([O-:29])=O)=[CH:23][CH:22]=2)[CH:17]=[CH:16][C:15]([C:18]([O-:20])=O)=[CH:14][CH:13]=1>>[O:8]1[CH:9]=[CH:10][CH:11]=[C:7]1[C:5]1[NH:4][N:3]=[C:2]([NH:1][C:27]([C:24]2[CH:23]=[CH:22][C:21]([C:12]3[CH:13]=[CH:14][C:15]([C:18]([NH:1][C:2]4[CH:6]=[C:5]([C:7]5[O:8][CH:9]=[CH:10][CH:11]=5)[NH:4][N:3]=4)=[O:20])=[CH:16][CH:17]=3)=[CH:26][CH:25]=2)=[O:29])[CH:6]=1Participants
3
Procedure
Compound 468 was prepared from 3-amino-5-(2-furanyl)pyrazole and 4,4′-biphenyldicarboxylate. [M+H]+ calcd for C28H21N6O4: 505.16; found: 504.93.
Sources & evidence
- ORD record
- ord-1f57933c01ae444c8c2c57a148894ad5
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09144557B2
Reaction notes
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