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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337439Generated: October 28, 2026

Isonicotinic Acid → HCID 23144600, compound

https://huagongshe.com/reaction/337439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsonicotinic AcidHCID 5922—
ReactantTriethylamineHCID 8471—
ReactantPyBOPHCID 2724699—
ReactantHCID 23144092HCID 23144092—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 23144600HCID 2314460025.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

2-Amino-5-(1-ethyl-2-oxo-1,2-dihydropyridin-5-yl)-4-(2-furyl)thiazole (287 mg, 1.00 mmol) obtained in Step 1 was dissolved in DMF (4 mL), and isonicotinic acid (246 mg, 2.00 mmol), PyBOP (1.14 g, 2.20 mmol) and triethylamine (0.613 mL, 4.40 mmol) were added thereto, followed by stirring at 80° C. for 1 hour. The reaction mixture was poured into water, followed by extraction with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate, and then the solvent was distilled away under reduced pressure. The resulting residue was purified through silica gel column chromatography (chloroform:methanol=17:1), followed by reslurrying with a mixed solvent of methanol and diethyl ether to afford the entitled Compound 127 (99.0 mg, 25%) as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889718B2
Source datasetuspto-grants-2014_11
ORD IDord-fc9dd1c6f67142b7b62faa50f9bde682
Source noteuspto-grants-2014_11