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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486289Generated: October 27, 2026

Triphenylphosphine → 2,5-Dimethyl-7-(3-methylbutoxy)pyrazolo[1,5-a]pyridine-3-carboxylic Acid ethyl Ester

https://huagongshe.com/reaction/1486289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantIsoamyl AlcoholHCID 31260—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 178469270HCID 178469270—
SolventTetrahydrofuranHCID 8028—
Solventtert-Butyl methyl etherHCID 15413—
Product2,5-Dimethyl-7-(3-methylbutoxy)pyrazolo[1,5-a]pyridine-3-carboxylic Acid ethyl EsterHCID 117864577—

Reaction Steps

A solution of 180 mg (0.768 mmol) of 7-hydroxy-2,5-dimethylpyrazolo[1,5-a]pyridine-3-carboxylic acid ethyl ester from Example 8A in 7 ml of dry tetrahydrofuran was admixed with 0.167 ml (1.537 mmol) of 3-methylbutan-1-ol (CAS 123-51-3), 423.2 mg (1.614 mmol) of triphenylphosphine and 0.32 ml (1.614 mmol) of diethyl azodicarboxylate. The resulting mixture was stirred at room temperature for 1 h. Some of the solvent was drawn off under reduced pressure and the residue was admixed with 5 ml of tert-butyl methyl ether. The resulting precipitate was filtered off and the mother liquor was partitioned between dichloromethane (15 ml) and water (10 ml). The organic phase was removed and concentrated under reduced pressure. The residue was purified by flash chromatography using a prepacked silica gel cartridge (eluent:cyclohexane-ethyl acetate 10:1 to 1:1), which gave 225 mg (69% of theory, 72% pure) of the target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422285B2
Source datasetuspto-grants-2016_08
ORD IDord-66538e5fc46d4126b51a0eef839a462f
Source noteuspto-grants-2016_08