Ammonia → 1-((2-(4-chlorophenyl)imidazo[1,2-a]pyridin-3-yl)methyl)-1H-1,2,4-triazole-3-carboxamide
Reaction equation
C[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]([O:52]C)=O)=[N:46]2)=[CH:31][CH:30]=1.N>>[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]([NH2:2])=[O:52])=[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 ammonia. 1H-NMR (D6-DMSO, 400 MHZ, d) 8.60 (d, J=6.9 Hz, 1H), 8.41 (s, 1H), 8.17 (s, 1H), 8.03 (s, 1H), 7.83 (d, J=8.5 Hz, 2H), 7.65 (d, J=9.1 Hz, 1H), 7.50 (d, J=8.5 Hz, 2H), 7.35 (t, J=7.9 Hz, 1H), 7.00 (t, J=6.8 Hz, 1H), 6.32 (s, 2H) ppm; m/e 353, 355.
Sources & evidence
- ORD record
- ord-8774c21cf1bc4b9ea52cc014602e357e
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08497278B2
Reaction notes
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