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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885059Generated: October 31, 2026

7-Chloro-4-methoxy-1H-pyrrolo[2,3-c]pyridine → 1-(4-methoxy-1H-pyrrolo[2,3-c]pyridin-7-yl)-1H-1,2,4-triazole-3-carbonitrile

https://huagongshe.com/reaction/885059

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Chloro-4-methoxy-1H-pyrrolo[2,3-c]pyridineHCID 15987013—
ReactantHCID 178510603HCID 178510603—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
Product1-(4-methoxy-1H-pyrrolo[2,3-c]pyridin-7-yl)-1H-1,2,4-triazole-3-carbonitrileHCID 5802603738%

Reaction Conditions

Temperature150 °C

Reaction Steps

7-Chloro-4-methoxy-1H-pyrrolo[2,3-c]pyridine (4 g, 21.90 mmol), 1H-1,2,4-triazole-3-carbonitrile (6.18 g, 65.7 mmol) and copper (I) iodide (1.252 g, 6.57 mmol) were combined in pyridine (6 mL) in a sealed tube. The mixture was heated to 150° C. for 6 hrs. After cooling to room temperature, the mixture was diluted with EtOAc (3000 mL), washed with 5% NaHCO3 (100 mL), brine (100 mL) and concentrated. The residue was purified by silica gel column using 30% EtOAc in hexanes mixture to give 1-(4-methoxy-1H-pyrrolo[2,3-c]pyridin-7-yl)-1H-1,2,4-triazole-3-carbonitrile (2 g, 8.33 mmol, 38.0% yield). LCMS: m/z 241.1 (M+H), 1.67 min (method 8).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242124B2
Source datasetuspto-grants-2012_08
ORD IDord-223b657cd7f14d8ba11728e870fcc519
Source noteuspto-grants-2012_08