Isocyanate → 1-[2-Fluoro-5-(trifluoromethyl)phenyl]-3-[4-({2-[({[2-fluoro-5-(trifluoromethyl)phenyl]amino}carbonyl)amino]imidazo[1,2-b]pyridazin-6-yl}ethynyl)phenyl]urea
Reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]#[C:9][C:10]2[CH:11]=[CH:12][C:13]3[N:14]([CH:16]=[C:17]([NH2:19])[N:18]=3)[N:15]=2)=[CH:4][CH:3]=1.[F:20][C:21]1[CH:26]=[CH:25][C:24]([C:27]([F:30])([F:29])[F:28])=[CH:23][C:22]=1[N:31]=[C:32]=[O:33].[N-:34]=[C:35]=[O:36]>>[F:20][C:21]1[CH:26]=[CH:25][C:24]([C:27]([F:30])([F:29])[F:28])=[CH:23][C:22]=1[NH:31][C:32]([NH:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]#[C:9][C:10]2[CH:11]=[CH:12][C:13]3[N:14]([CH:16]=[C:17]([NH:19][C:35]([NH:34][C:22]4[CH:23]=[C:24]([C:27]([F:29])([F:30])[F:28])[CH:25]=[CH:26][C:21]=4[F:20])=[O:36])[N:18]=3)[N:15]=2)=[CH:4][CH:3]=1)=[O:33]Participants
4
Reactant 3
Product 1
Procedure
The compound of Example 10 was made by preparing 6-[(4-aminophenyl)ethynyl]imidazo[1,2-b]pyridazin-2-amine as in Example 20, followed by a procedure similar to Example 3 using 1-fluoro-2-isocyanato-4-(trifluoromethyl)benzene as the isocyanate (see also Schemes 1, 2, and 9).
Sources & evidence
- ORD record
- ord-aa66ad06f54d44cf88a1d004678b1a8f
- Source dataset
- uspto-grants-2016_01
- Patent number
- US09233968B1
Reaction notes
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