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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361790Generated: October 30, 2026

Isonicotinic Acid → HCID 23144222, compound

https://huagongshe.com/reaction/1361790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsonicotinic AcidHCID 5922—
ReactantTriethylamineHCID 8471—
ReactantPyBOPHCID 2724699—
ReactantHCID 23144139HCID 23144139—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 23144222HCID 2314422237%

Reaction Conditions

Temperature80 °C

Reaction Steps

2-Amino-5-(1-ethyl-2-oxo-1,2-dihydropyridin-4-yl)-4-(2-furyl)thiazole (167 mg, 0.582 mmol) obtained in Step 1 was dissolved in DMF (8 mL), and isonicotinic acid (143 mg, 1.16 mmol), PyBOP (664 mg, 1.28 mmol) and triethylamine (0.356 mL, 2.55 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 124 (83.5 mg, 37%) as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880013B2
Source datasetuspto-grants-2011_02
ORD IDord-87bfac10505148d3b54c8c2a09b97367
Source noteuspto-grants-2011_02