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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783388Generated: October 30, 2026

1H-1,2,4-Triazole → 4-Methoxy-7-(1,2,4-triazol-1-yl)-6-azaindole

https://huagongshe.com/reaction/1783388

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantPotassium HydroxideHCID 14797—
Reactant7-Chloro-4-methoxy-1H-pyrrolo[2,3-c]pyridineHCID 15987013—
CatalystCopperHCID 23978—
SolventMethanolHCID 887—
Product4-Methoxy-7-(1,2,4-triazol-1-yl)-6-azaindoleHCID 2079125058%

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of 7-chloro-4-methoxy-6-azaindole (1.029 g, 5.62 mmol), 1,2,4-triazole (11.6 g, 30 equiv), copper bronze (0.72 g, 11.2 mgatom) and finely pulverized KOH (0.63 g, 11.2 mmol) was heated in a sealed tube at 160° C. (oil bath temperature) for 18 h. The cooled mixture was taken up in MeOH and the resulting slurry was filtered through a pad of Celite. The filtrate was evaporated, the residue taken up in EtOAc and the resulting suspension was filtered. This process was repeated and the resulting solution was susequently adsorbed on silica gel and the volatiles were removed in vacuo. This solid was applied to the top of a silica gel chromatography column, which was eluted with 10-50% EtOAc—CH2Cl2 to give the title compound (0.697 g, 58%) as an off-white solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501419B2
Source datasetuspto-grants-2009_03
ORD IDord-67bc241e82b741dfbd05c329de930cf6
Source noteuspto-grants-2009_03