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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925557Generated: October 28, 2026

Hydrochloric Acid → 2-(3,3-Difluoro-3-(4-fluorophenyl)propylthio)-nicotinic acid

https://huagongshe.com/reaction/1925557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(3-Bromo-1,1-difluoropropyl)-4-fluorobenzeneHCID 67133822—
ReactantHCID 178524460HCID 178524460—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl acetate hexaneHCID 21226206—
Product2-(3,3-Difluoro-3-(4-fluorophenyl)propylthio)-nicotinic acidHCID 6713367431%

Reaction Conditions

Temperature90 °C

Reaction Steps

1.02 g (4.0 mmol) of 1-(3-bromo-1,1-difluoropropyl)-4-fluorobenzene (precursor VC005) and 1.67 g (12.0 mmol) of K2CO3 were added to a solution of 620 mg (4.0 mmol) of 2-mercapto-nicotinic acid in DMF (10 ml), and the mixture was heated for 2 h at 90° C. Dilution with water (20 ml) was then carried out, and the pH was adjusted to −2 with 6M hydrochloric acid. Extraction with EA (3×40 ml) was then carried out. The combined organic phases were washed with water and brine, dried over Na2SO4, filtered and concentrated in vacuo. CC (hexane/EA 1:4) of the residue yielded 400 mg (1.2 mmol, 31%) of 2-(3,3-difluoro-3-(4-fluorophenyl)propylthio)-nicotinic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178684B2
Source datasetuspto-grants-2012_05
ORD IDord-911744400e8541d399fa041ec0d9d740
Source noteuspto-grants-2012_05