3-Methoxy-5-(pentafluoro-lambda6-sulphanyl)benzoic acid → 3-Methoxy-N-{4-methyl-3-[6-(pyridin-3-yl)-1H-imidazo[1,2-b]pyrazol-1-yl]phenyl}-5-(penta-fluoro-lambda6-sulphanyl)benzamide
Reaction equation
[CH3:1][C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[CH:4][C:3]=1[N:9]1[C:16]2[N:12]([N:13]=[C:14]([C:17]3[CH:18]=[N:19][CH:20]=[CH:21][CH:22]=3)[CH:15]=2)[CH:11]=[CH:10]1.[CH3:23][O:24][C:25]1[CH:26]=[C:27]([CH:31]=[C:32]([S:34]([F:39])([F:38])([F:37])([F:36])[F:35])[CH:33]=1)[C:28](O)=[O:29]>>[CH3:23][O:24][C:25]1[CH:26]=[C:27]([CH:31]=[C:32]([S:34]([F:39])([F:35])([F:36])([F:37])[F:38])[CH:33]=1)[C:28]([NH:6][C:5]1[CH:7]=[CH:8][C:2]([CH3:1])=[C:3]([N:9]2[C:16]3[N:12]([N:13]=[C:14]([C:17]4[CH:18]=[N:19][CH:20]=[CH:21][CH:22]=4)[CH:15]=3)[CH:11]=[CH:10]2)[CH:4]=1)=[O:29]Participants
3
Reactant 2
Product 1
Procedure
30 mg (0.10 mmol) of the compound of Example 6A and 29 mg (0.10 mmol) of the compound of Example 25A were reacted and worked up analogously to the procedure of Example 16. This gave 32 mg (55% of theory) of the title compound.
Sources & evidence
- ORD record
- ord-ca88e15fd3b94704bbdeb0b6b3212d63
- Source dataset
- uspto-grants-2016_07
- Patent number
- US09394309B2
Reaction notes
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