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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181155Generated: November 1, 2026

3-Bromopyridine → HCID 69588948, compound

https://huagongshe.com/reaction/2181155

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromopyridineHCID 12286—
Reactant(S)-N-Boc-2-ethynylpyrrolidineHCID 11030701—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Catalystpalladium(II) acetateHCID 167845—
CatalystHCID 178418397HCID 178418397—
ProductHCID 69588948HCID 6958894871.7%

Reaction Conditions

Temperature60 °C

Reaction Steps

Triethylamine (10 mL) was degassed by bubbling argon over a period of 30 min. (S)-N-(tert-butoxycarbonyl)-2-ethynylpyrrolidine (1.00 g, 5.12 mmol), tetrakis(triphenylphosphine)palladium (0.296 g, 0.256 mmol), palladium(II) acetate (0.0575 g, 0.256 mmol), copper (I) iodide (16.2 mg, 0.085 mmol) and 5-bromopyridine (2.43 g, 15.4 mmol) were added. The mixture was heated at 60° C. for 24 h, then cooled to room temperature and concentrated by rotary evaporation. The residue was dissolved in chloroform (50 mL) and the organic phase washed sequentially with water (25 mL), saturated aqueous NaHCO3 solution (3×20 mL) and water (25 mL). The solution was then dried (MgSO4), filtered and concentrated by rotary evaporation. The crude product was purified by column chromatography on silica gel, eluting with ethyl acetate/hexane (1/1, v/v). Selected fractions containing the product were concentrated via rotary evaporation to give 1.00 g (71%) of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06890935B2
Source datasetuspto-grants-2005_05
ORD IDord-d5aa7431254c4abd98817a4981d8d91d
Source noteuspto-grants-2005_05