3-Phenylprop-2-enenitrile → 2,7-Diphenyl-[1,2,4]triazolo[1,5-a]pyridin-5-ylamine

HRID 277036Notes

Reaction equation

HRID 277036 reaction equation
C1(S([CH2:10][C:11]2[N:15]=[C:14]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)[NH:13][N:12]=2)(=O)=O)C=CC=CC=1.[C:22](#[N:31])[CH:23]=[CH:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1>>[C:16]1([C:14]2[N:15]=[C:11]3[CH:10]=[C:24]([C:25]4[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=4)[CH:23]=[C:22]([NH2:31])[N:12]3[N:13]=2)[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1

Participants

3

Reactant 2

HCID 746673-Phenylprop-2-enenitrileHCID 1785273983-benzenesulfonylmethyl-5-phenyl-1H-[1,2,4]triazole

Product 1

HCID 183136362,7-Diphenyl-[1,2,4]triazolo[1,5-a]pyridin-5-ylamine

Procedure

The title compound, mp. 214-216° C., was prepared in accordance with the general method of example 22 from 3-benzenesulfonylmethyl-5-phenyl-1H-[1,2,4]triazole and cinnamonitrile.

Sources & evidence

ORD record
ord-89284d80fe36467c8064146a0b94394a
Source dataset
uspto-grants-2002_03
Patent number
US06355653B1

Reaction notes

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