Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250462Generated: October 26, 2026

Potassium Cyanide → 5-(3-Chlorothiophen-2-yl)-3-(4-chloro-3-cyano-phenyl)-[1,2,4]-oxadiazole

https://huagongshe.com/reaction/2250462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
ReactantSodium CarbonateHCID 10340—
Reactant2-Chloro-5-[5-(3-chlorothiophen-2-yl)-[1,2,4]oxadiazol-3-yl]-phenylamineHCID 9995637—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
SolventEthyl AcetateHCID 8857—
Product5-(3-Chlorothiophen-2-yl)-3-(4-chloro-3-cyano-phenyl)-[1,2,4]-oxadiazoleHCID 1035873222%

Reaction Steps

A solution of sodium nitrite (76.8 mg, 1.11 mmol) and water (650 μL) was added dropwise to a stirred suspension of 3-(3-amino-4-chloro-phenyl)-5-(3-chlorothiophen-2-yl)-[1,2,4]-oxadiazole (335 mg, 1.07 mmol) in sulfuric acid (3.0 mL), water (8 mL) and some crushed ice in an ice bath. The solution was stirred for 1.25 h and then was poured into a solution of cuprous cyanide (152 mg, 1.70 mmol), potassium cyanide (231 mg, 3.55 mmol) and water (8 mL) in an ice bath. The solution was stirred for 10 min, then ethyl acetate (50 mL) was added, followed by sodium carbonate to bring the solution to pH 7, and the solution was equilibrated to room temperature. The ethyl acetate layer was concentrated by rotary evaporation and the product was purified by column chromatography to yield 75.7 mg (22%) of the title compound as a light yellow solid. 1H NMR (CDCl3): 8.49 (d, J=2.20 Hz, 1H), 8.33 (dd, J1=8.52 Hz, J2=2.20 Hz, 1H), 7.67 (m, 2H), 7.16 (d, J=5.50 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317029B2
Source datasetuspto-grants-2008_01
ORD IDord-d84e9bb5aae9424b8f13c7117f460653
Source noteuspto-grants-2008_01