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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451452Generated: October 30, 2026

Dichloromethane → HCID 67337313, compound

https://huagongshe.com/reaction/451452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium CarbonateHCID 10340—
Reactant4-Chlorophenylboronic acidHCID 74299—
ReactantHCID 67335149HCID 67335149—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67337313HCID 67337313—

Reaction Steps

To a solution of 2-(2-amino-8-bromo-[1,2,4]triazolo[1,5-a]pyridin-5-yl)-propan-2-ol (contaminated with ketone) (120 mg, 0.443 mmol) and 4-chlorophenyl boronic acid (155 mg, 0.987 mmol) in dioxane (6 mL) was added aqueous solution of Na2CO3 (2 M, 0.72 mL) and degassed with argon for 5 minute. To this was added PdCl2 (dppf)2.CH2Cl2 (30.34 mg, 0.04 mmol) and stirred at 90° C. for 90 minutes. The reaction mixture was cooled to room temperature and water (20 mL) was added. The aqueous phase was extracted with ethyl acetate, the combined organic phases were dried over sodium sulfate, the solvent was evaporated and the residue was purified by silica gel chromatography using ethyl acetate/hexane as eluent. The title compound was obtained as an off white solid (65 mg, 48%) which was contaminated with 1-[2-amino-8-(4-chloro-phenyl)-[1,2,4]triazolo[1,5-a]pyridin-5-yl]-ethanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486967B2
Source datasetuspto-grants-2013_07
ORD IDord-7fcf56dc98744dd58cceac0342f40f38
Source noteuspto-grants-2013_07