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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337507Generated: October 27, 2026

Sodium Bicarbonate → N-[4-(2-Furyl)-5-(tetrahydropyran-4-ylcarbonyl)thiazol-2-yl]tetrahydrofuran-3-carboxamide

https://huagongshe.com/reaction/337507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant(R)-Tetrahydro-3-furoic acidHCID 4661317—
Reactant2-Amino-4-(2-furyl)-5-(tetrahydropyran-4-ylcarbonyl)thiazoleHCID 86612468—
ProductN-[4-(2-Furyl)-5-(tetrahydropyran-4-ylcarbonyl)thiazol-2-yl]tetrahydrofuran-3-carboxamideHCID 2314423584%

Reaction Conditions

Temperature60 °C

Reaction Steps

Tetrahydrofuran-3-carboxylic acid (1.72 mL, 1.8 mmol), EDC hydrochloride (344 mg, 1.80 mmol) and 1-hydroxybenzotriazole monohydrate (276 mg, 1.80 mmol) were added to Compound 454 (125 mg, 0.450 mmol), followed by stirring at 60° C. for 3.5 hours. The reaction mixture was poured into a saturated aqueous solution of sodium hydrogencarbonate, 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 reslurried with diethyl ether to afford the entitled Compound 524 (142 mg, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889718B2
Source datasetuspto-grants-2014_11
ORD IDord-f15067f383364eea837628d129b5fdfb
Source noteuspto-grants-2014_11