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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1041835Generated: October 31, 2026

Tetrahydrofuran → HCID 178519734, compound

https://huagongshe.com/reaction/1041835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-(Benzyloxy)-6-oxo-1,6-dihydropyridine-2-carboxylic acidHCID 15450555—
ReactantHCID 178527880HCID 178527880—
ProductHCID 178519734HCID 17851973483.7%

Reaction Steps

To a solution of 1-benzyloxy-6-carboxy-2 (1H)-pyridinone (4.90 g, 20 mmol), 2-mercaptothiazoline (2.62 g, 22 mmol), and a catalytic amount of 4-dimethyl-aminopyridine (DMAP) in dry THF (50 mL), was added N,N′-dicyclohexylcarbodiimide (DCC) (4.6 g, 22 mmol). After stirring overnight, the dicyclohexylurea (DCU) solids are removed by filtration the yellow filtrate is removed by rotary evaporation to give a yellow solid. Crystallization from isopropanol-methylene chloride gives the title compound (5.80 g, 83.7%) as a pale yellow powder, m.p.: 135-7° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557601B2
Source datasetuspto-grants-2013_10
ORD IDord-37b0709f14574092ad760bcf8171185e
Source noteuspto-grants-2013_10