Cinnolin-5-amine → N-Cinnolin-5-yl-N'-[4-(trifluoromethyl)benzyl]urea
Reaction equation
[N:1]1[C:10]2[CH:9]=[CH:8][CH:7]=[C:6]([NH2:11])[C:5]=2[CH:4]=[CH:3][N:2]=1.[F:12][C:13]([F:25])([F:24])[C:14]1[CH:23]=[CH:22][C:17]([CH2:18][N:19]=[C:20]=[O:21])=[CH:16][CH:15]=1>>[N:1]1[C:10]2[C:5](=[C:6]([NH:11][C:20]([NH:19][CH2:18][C:17]3[CH:16]=[CH:15][C:14]([C:13]([F:12])([F:25])[F:24])=[CH:23][CH:22]=3)=[O:21])[CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][N:2]=1Participants
3
Procedure
Prepared from cinnolin-5-amine (Sci Pharm. 1982, 50, 246) and [4-(trifluoromethyl)benzyl]isocyanate (Description 58) according to the procedure of Description 61. m/z (ES+) 347 (M+H)+.
Sources & evidence
- ORD record
- ord-62b79cc006ba4d1387f8bc5b847e6732
- Source dataset
- uspto-grants-2007_10
- Patent number
- US07285563B2
Reaction notes
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