Methylamine → 1-((2-(4-chlorophenyl)imidazo[1,2-a]pyridin-3-yl)methyl)-N-methyl-1H-1,2,4-triazole-3-carboxamide
Reaction equation
[CH3:1][NH:2]C(C1N(CC2N3C=C(C)C=CC3=NC=2C2C=CC(C)=CC=2)N=CN=1)=O.[Cl:28][C:29]1[CH:34]=[CH:33][C:32]([C:35]2[N:36]=[C:37]3[CH:42]=[CH:41][CH:40]=[CH:39][N:38]3[C:43]=2[CH2:44][N:45]2[CH:49]=[N:48][C:47]([C:50](OC)=[O:51])=[N:46]2)=[CH:31][CH:30]=1.CN>>[Cl:28][C:29]1[CH:34]=[CH:33][C:32]([C:35]2[N:36]=[C:37]3[CH:42]=[CH:41][CH:40]=[CH:39][N:38]3[C:43]=2[CH2:44][N:45]2[CH:49]=[N:48][C:47]([C:50]([NH:2][CH3:1])=[O:51])=[N:46]2)=[CH:31][CH:30]=1Participants
4
Reactant 3
Product 1
Procedure
The title compound was prepared according to the procedure described for compound 68 from methyl 1-((2-(4-chlorophenyl)imidazo[1,2-a]pyridin-3-yl)methyl)-1H-1,2,4-triazole-3-carboxylate and methylamine. 1H-NMR (400 MHz, CDCl3, δ) 8.42 (d, J=6.8 Hz, 1H), 7.98 (d, J=8.5 Hz, 2H), 7.85 (s, 1H), 7.69 (d, J=9.1 Hz, 1H), 7.50 (broad, 1H), 7.45 (d, J=8.5 Hz, 2H), 7.29 (m, 1H), 6.87 (m, 1H), 6.34 (s, 2H), 3.08 (d, J=5.1 Hz, 3H) ppm; m/e 367, 369.
Sources & evidence
- ORD record
- ord-85e1753118624b76861cda2692f57575
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08497278B2
Reaction notes
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