m-Anisoyl chloride → 3-Methoxy-N-(5-methoxy-8-phenyl-[1,2,4]triazolo[1,5-a]pyridin-2-yl)-benzamide

HRID 2120763Notes

Reaction equation

HRID 2120763 reaction equation
[CH3:1][O:2][C:3]1[N:8]2[N:9]=[C:10]([NH2:12])[N:11]=[C:7]2[C:6]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[CH:5][CH:4]=1.[CH3:19][O:20][C:21]1[CH:22]=[C:23]([C:27](Cl)=[O:28])[CH:24]=[CH:25][CH:26]=1>>[CH3:19][O:20][C:21]1[CH:22]=[C:23]([CH:24]=[CH:25][CH:26]=1)[C:27]([NH:12][C:10]1[N:11]=[C:7]2[C:6]([C:13]3[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=3)=[CH:5][CH:4]=[C:3]([O:2][CH3:1])[N:8]2[N:9]=1)=[O:28]

Participants

3

Reactant 2

HCID 74374m-Anisoyl chlorideHCID 234358815-Methoxy-8-phenyl-[1,2,4]triazolo[1,5-a]pyridin-2-yl-amine

Product 1

HCID 234358873-Methoxy-N-(5-methoxy-8-phenyl-[1,2,4]triazolo[1,5-a]pyridin-2-yl)-benzamide

Procedure

According to example 6, the title compound was synthesized from 5-methoxy-8-phenyl-[1,2,4]triazolo[1,5-a]pyridin-2-yl-amine and 3-methoxy-phenyl carboxylic acid chloride. (MS m/e (%): 374.4 (M+H+, 100).

Sources & evidence

ORD record
ord-e4c8ee33b2d24fc7a0ac9d7c6e89f478
Source dataset
uspto-grants-2004_02
Patent number
US06693116B2

Reaction notes

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