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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 431944Generated: October 30, 2026

Dichloromethane → 5-(2-Pyridyl)-3-[3-(3-pyridyl)-phenyl]-1,2,4-oxadiazole hydrochloride

https://huagongshe.com/reaction/431944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium CarbonateHCID 10340—
Reactant3-(1,3,2-Dioxaborinan-2-yl)pyridineHCID 4198005—
Reactant3-(3-Iodophenyl)-5-(2-pyridyl)-1,2,4-oxadiazoleHCID 21942596—
CatalystHCID 178418789HCID 178418789—
ProductHydrochloric AcidHCID 313—
Product5-(2-Pyridyl)-3-[3-(3-pyridyl)-phenyl]-1,2,4-oxadiazole hydrochlorideHCID 1876154255.45%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 3-(3-iodophenyl)-5-(2-pyridyl)-1,2,4-oxadiazole (55 mg, 0.158 mmol), pyridine-3-boronic acid 1,3-propanediol cyclic ester (51.4 mg, 0.3152 mmol), and tetrakis(triphenylphosphine)palladium(0) Pd(PPh3)4, 25 mg, 0.0216 mmol), in a solution of ethylene glycol dimethyl ether (1.5 mL) and 2M sodium carbonate (1.5 mL) was heated in a sealed vial at 100° C. for 1 hour. The reaction was cooled, diluted with dichloromethane, washed with water and saturated brine, filtered, and concentrated. Silica gel chromatography using 40% and 60% ethyl acetate in hexane and then the treatment of 1M HCl (0.2 mL) afforded 29.4 mg (55.45%) 5-(2-pyridyl)-3-[3-(3-pyridyl)-phenyl]-1,2,4-oxadiazole hydrochloride. 1H-NMR (CDCl3), δ (ppm): 9.34 (s, 1H), 8.88 (m, 3H), 8.54 (s, 1H), 8.40 (d, 1H), 8.28 (d, 1H), 8.16 (d, 1H), 8.00 (m, 3H), 7.82 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660753B2
Source datasetuspto-grants-2003_12
ORD IDord-f915018ab8c342d4a219369becf51edd
Source noteuspto-grants-2003_12