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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177643Generated: October 29, 2026

Aniline → 7-methyl-1-phenyl-1H-[1,2,3]triazolo[4,5-c]pyridine

https://huagongshe.com/reaction/2177643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
Reactant2-AminopyridineHCID 10439—
Reactant4-Chloro-3-nitropyridineHCID 2735781—
Reactant4-Chloro-3-methyl-5-nitropyridineHCID 58882371—
Product7-methyl-1-phenyl-1H-[1,2,3]triazolo[4,5-c]pyridineHCID 90410064—

Reaction Steps

The title compound was prepared in a manner analogous to Intermediate 17, Step 1 through Intermediate 19, Step 3 substituting 4-chloro-3-methyl-5-nitro-pyridine for 4-chloro-3-nitropyridine, and aniline for 2-aminopyridine. MS (ESI) mass calcd. C12H10N4, 210.1. m/z found, 225.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09066946B2
Source datasetuspto-grants-2015_06
ORD IDord-c9f68a9b1b97435d892bcb3d42653eeb
Source noteuspto-grants-2015_06