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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580522Generated: October 31, 2026

4-Fluorobenzoic Acid → HCID 20134105, compound

https://huagongshe.com/reaction/580522

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzoic AcidHCID 9973—
ReactantHexamethylphosphoramideHCID 12679—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 67938339HCID 67938339—
SolventAcetonitrileHCID 6342—
SolventSodium BicarbonateHCID 516892—
ProductHCID 20134105HCID 20134105—

Reaction Steps

To a solution of 308 mg of 4-fluorobenzoic acid in 5 ml of anhydrous hexamethylphosphoramide and 0.5 ml of anhydrous acetonitrile is added dropwise 250 mg of thionyl chloride at -5°-0° C. under nitrogen. After stirring at the same temperature for 30 minutes, 358 mg of diaminothienopyridine D1 is added and stirred at O°-5° C. for 3 hours. The mixture is diluted with ice-water and neutralized with saturated aqueous sodium bicarbonate. The resulting crystals are filtered, washed with water and dried to yield 630 mg of 4-amino-2-methyl-5-(4-fluorobenzoylamino)thieno[2,3-b]pyridine E1. It is suspended in 15 ml of polyphosphoric acid and heated at 140° C. with stirring under nitrogen. The cooled mixture is poured into ice-water and neutralized with aqueous sodium hydroxide. The product is extracted with ethyl acetate and the extract is washed with water, dried and evaporated. The residue is chromatographed on silica gel with chloroform-methanol (25:1 v/v) as eluent to afford 457 mg (81%) of F1 as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04753951
Source datasetuspto-grants-1988_06
ORD IDord-d3a8b4da8cc243d683ed70ff82078f24
Source noteuspto-grants-1988_06