Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830867Generated: October 30, 2026

Tetrahydrofuran → HCID 22049707, compound

https://huagongshe.com/reaction/1830867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl 5-bromopyridine-3-carboxylateHCID 140785—
Reactant2-Bromo-4-(4-chlorophenyl)-1,3-thiazoleHCID 22049747—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418397HCID 178418397—
ProductHCID 22049707HCID 2204970751%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of compound (41) (0.25 g, 0.91 mmol) in tetrahydrofuran (5 ml) was cooled to −78° C. under an argon atmosphere and 1.6 M n-butyllithium-hexane solution (0.57 ml, 0.91 mmol) was added. After stirring at −78° C. for 30 min., a solution of zinc chloride (0.12 g, 0.91 mmol) in tetrahydrofuran (2 ml) was added to the reaction mixture. The reaction mixture was warmed to room temperature and stirred for 30 min. and ethyl 5-bromonicotinate (0.21 g, 0.91 mmol) and tetrakis(triphenylphosphine)palladium (0.16 g, 0.14 mmol) were added. The mixture was heated to 75° C. and stirred for 2 hrs. After cooling, the reaction mixture was poured into ice water and partitioned between ethyl acetate and brine. The aqueous layer was extracted with ethyl acetate and the extracts were combined and dried (MgSO4), and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography, and crystallized from ethyl acetate-n-hexane to give white crystals (0.16 g, 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067537B2
Source datasetuspto-grants-2006_06
ORD IDord-a3de0a11f79645059b0888b511d5f4cc
Source noteuspto-grants-2006_06