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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525830Generated: October 30, 2026

Water → 3-Hydroxypropyl 7-{3-[(3-methyl-2-furoyl)amino]phenoxy}thieno[3,2-b]pyridine-2-carboxylate

https://huagongshe.com/reaction/525830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Bromo-1-propanolHCID 12308—
Reactant7-{3-[(3-Methyl-2-furoyl)amino]phenoxy}thieno[3,2-b]pyridine-2-carboxylic acidHCID 86290323—
SolventDimethylformamideHCID 6228—
Product3-Hydroxypropyl 7-{3-[(3-methyl-2-furoyl)amino]phenoxy}thieno[3,2-b]pyridine-2-carboxylateHCID 86290371—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of 7-{3-[(3-methyl-2-furoyl)amino]phenoxy}thieno[3,2-b]pyridine-2-carboxylic acid (120 mg, 0.30 mmol) in anhydrous DMF (10 ml) were added 3-bromo-1-propanol (63 mg, 0.45 mmol) and potassium carbonate (83 mg, 0.60 mmol). The mixture was heated at 50° C. for 5 hours and poured into 100 ml of water. The precipitates were filtered, washed with water and dried to give the crude, which was purified by silica gel chromatography eluting with 3˜5% of methanol in chloroform to give 3-hydroxypropyl 7-{3-[(3-methyl-2-furoyl)amino]phenoxy}thieno[3,2-b]pyridine-2-carboxylate as white solid. Yield: 25 mg, 18%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340555B2
Source datasetuspto-grants-2016_05
ORD IDord-e6b3028434254c8895e9b5bed43405e5
Source noteuspto-grants-2016_05