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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726331Generated: October 28, 2026

5-Bromo-2-furanecarboxylic acid → HCID 952706, compound

https://huagongshe.com/reaction/1726331

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2-furanecarboxylic acidHCID 68511—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant(R)-(+)-3-Aminoquinuclidine DihydrochlorideHCID 12494972—
SolventDimethylformamideHCID 6228—
ProductHCID 952706HCID 95270654.7%

Reaction Steps

A mixture of (R)-1-azabicyclo[2.2.2]oct-3-ylamine dihydrochloride (655 mg), 5-bromofuran-2-carboxylic acid (681 mg), 1-hydroxybenzotriazole hydrate (457 mg), O-benzotriazol-1-yl-N,N,N′-tetramethyluronium tetrafluoroborate (1.069 g), and N,N-diisopropylethylamine (2.5 mL) in N,N-dimethylformamide (10 mL) was agitated until a homogenous solution was obtained, and was then allowed to stand at room temperature overnight. The solution was evaporated, and the residue was partitioned between aqueous sodium hydroxide and chloroform. The chloroform layer was dried over magnesium sulfate, filtered, and evaporated and the residue was purified by chromatography on silica gel in a solid phase extraction cartridge using ammoniated methanol/chloroform mixtures as the eluent. The compound was then dissolved in tetrahydrofuran (20 mL), excess hydrogen chloride (5 mL; 1M solution in diethyl ether) was added, and the solution was evaporated and then recrystallised from methanol/diethyl ether to give the hydrochloride salt of the title compound as a colourless solid (538 mg); MS (ES+) 299, 301 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491734B2
Source datasetuspto-grants-2009_02
ORD IDord-5e925204314249aeb00108400c6d4444
Source noteuspto-grants-2009_02