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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643672Generated: October 29, 2026

Ethanol → 3-(3-(2-Chlorophenyl)-[1,2,4]triazolo[4,3-a]pyridin-7-yl)-4-methylbenzoic acid

https://huagongshe.com/reaction/643672

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant3-Borono-4-methylbenzoic acidHCID 18980142—
Reactant7-Chloro-3-(2-chlorophenyl)-[1,2,4]triazolo[4,3-a]pyridineHCID 49871671—
CatalystHCID 178418476HCID 178418476—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product3-(3-(2-Chlorophenyl)-[1,2,4]triazolo[4,3-a]pyridin-7-yl)-4-methylbenzoic acidHCID 59261363—

Reaction Steps

A mixture of 7-chloro-3-(2-chlorophenyl)-[1,2,4]triazolo[4,3-a]pyridine (1.77 g, 6.7 mmol), 3-borono-4-methylbenzoic acid (1.57 g, 8.7 mmol), Pd(PPh3)2Cl2 (0.329 g, 0.46 mmol, Strem), and sodium carbonate (2.13 g, 20 mmol, JT Baker) in DME:EtOH:H2O=7:2:3 (8 ml) was heated to 80° C. for 8 h. The mixture was cooled to room temperature, diluted with MeOH and filtered through Celite. The filtrate was concentrated to yield the title compound as a brown solid. MS (ESI, pos. ion) m/z: 364.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700593B2
Source datasetuspto-grants-2010_04
ORD IDord-751a1a3676684f27a7aded26bdfbce68
Source noteuspto-grants-2010_04