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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242169Generated: October 31, 2026

1,3-Dichloroacetone → 2'-Amino-6'-[({2-[(3-chloro-4-fluorophenyl)amino]-1,3-thiazol-4-yl}methyl)thio]-6-(2-hydroxyethoxy)-3,4'-bipyridine-3',5'-dicarbonitrile

https://huagongshe.com/reaction/242169

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DichloroacetoneHCID 10793—
ReactantSodium BicarbonateHCID 516892—
Reactant(3-Chloro-4-fluorophenyl)thioureaHCID 704698—
ReactantHCID 178510485HCID 178510485—
SolventDimethylformamideHCID 6228—
Product2'-Amino-6'-[({2-[(3-chloro-4-fluorophenyl)amino]-1,3-thiazol-4-yl}methyl)thio]-6-(2-hydroxyethoxy)-3,4'-bipyridine-3',5'-dicarbonitrileHCID 24752906—

Reaction Conditions

Temperature80 °C

Reaction Steps

209 mg (0.67 mmol) of 4-fluoro-3-chlorophenylthiourea and 89 mg (0.70 mmol) of 1,3-dichloroacetone are dissolved in 5 ml of DMF, and the reaction solution is stirred at 80° C. for 3 h. After cooling, 209 mg (0.67 mmol) of the compound from example 2A and 224 mg (2.67 mmol) of sodium bicarbonate are added, and the mixture is stirred at RT for a further 20 h. The mixture is then filtered through a paper filter, and sat. sodium bicarbonate solution (5 ml) is added to the filtrate. The aqueous phase is extracted with ethyl acetate (three times, 5 ml each). The combined organic phases are dried over sodium sulphate, and the solvent is removed on a rotary evaporator.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653109B2
Source datasetuspto-grants-2014_02
ORD IDord-dab2dc9de9024257854fee9ff8b76989
Source noteuspto-grants-2014_02