Methylamine → HCID 59321028, compound
Reaction equation
[CH3:1][C:2]1O[C:5]([C:7]2[CH:12]=[CH:11][N:10]3[C:13]([C:16]4[CH:17]=[C:18]([NH:22][C:23]([NH:25][CH2:26][C:27]([F:30])([F:29])[F:28])=[O:24])[CH:19]=[CH:20][CH:21]=4)=[CH:14][N:15]=[C:9]3[CH:8]=2)=[N:4][N:3]=1.[CH3:31][NH2:32]>>[CH3:31][N:32]1[C:2]([CH3:1])=[N:3][N:4]=[C:5]1[C:7]1[CH:12]=[CH:11][N:10]2[C:13]([C:16]3[CH:17]=[C:18]([NH:22][C:23]([NH:25][CH2:26][C:27]([F:30])([F:29])[F:28])=[O:24])[CH:19]=[CH:20][CH:21]=3)=[CH:14][N:15]=[C:9]2[CH:8]=1Participants
3
Procedure
Alternatively the title compound could be prepared through reaction of 1-{3-[7-(5-methyl-[1,3,4]oxadiazol-2-yl)-imidazo[1,2-a]pyridin-3-yl]-phenyl}-3-(2,2,2-trifluoro-ethyl)-urea with methylamine.
Sources & evidence
- ORD record
- ord-d462d7d674de45f2bfb92c46147f2191
- Source dataset
- uspto-grants-2014_11
- Patent number
- US08895745B2
Reaction notes
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