(Z)-3-(6-chloro-pyridin-3-yl)-acrylonitrile → 7-(6-Chloro-pyridin-3-yl)-2-pyridin-2-yl-[1,2,4]triazolo[1,5-a]pyridin-5-ylamine
Reaction equation
C1(S([CH2:10][C:11]2[N:12]=[C:13]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][N:17]=3)[NH:14][N:15]=2)(=O)=O)C=CC=CC=1.[Cl:22][C:23]1[N:28]=[CH:27][C:26](/[CH:29]=[CH:30]\[C:31]#[N:32])=[CH:25][CH:24]=1>>[Cl:22][C:23]1[N:28]=[CH:27][C:26]([C:29]2[CH:30]=[C:31]([NH2:32])[N:15]3[N:14]=[C:13]([C:16]4[CH:21]=[CH:20][CH:19]=[CH:18][N:17]=4)[N:12]=[C:11]3[CH:10]=2)=[CH:25][CH:24]=1Participants
3
Procedure
The title compound, MS m/e (%):323 (M+H+,100), was prepared in accordance with the general method of example 1 from 2-(5-benzenesulfonylmethyl-2H-[1,2,4]triazol-3-yl)-pyridine and (E)/(Z)-3-(6-chloro-pyridin-3-yl)-acrylonitrile.
Sources & evidence
- ORD record
- ord-d538b6ba25f2488393cf6879c124dcde
- Source dataset
- uspto-grants-2002_03
- Patent number
- US06355653B1
Reaction notes
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