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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631302Generated: November 1, 2026

1-Butanol → HCID 86664565, compound

https://huagongshe.com/reaction/1631302

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ButanolHCID 263—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl 5-chloropyrazolo(1,5-a)pyrimidine-3-carboxylateHCID 58063474—
Reactant(R)-5-fluoro-2-methoxy-3-(pyrrolidin-2-yl)pyridine dihydrochlorideHCID 66847679—
SolventEthyl AcetateHCID 8857—
ProductHCID 86664565HCID 8666456556.3%

Reaction Steps

Ethyl 5-chloropyrazolo[1,5-a]pyrimidine-3-carboxylate (Preparation B, 0.75 g, 3.32 mmol), (R)-5-fluoro-2-methoxy-3-(pyrrolidin-2-yl)pyridine dihydrochloride (0.984 g, 3.66 mmol), diisopropylethylamine (2.32 mL, 13.3 mmol) and n-butanol (1.11 mL) were heated at 90° C. for 48 hours. The reaction mixture was diluted with EtOAc and the mixture was washed with water, brine and saturated NaHCO3. The organic layer was dried with MgSO4, filtered and concentrated afford a dark orange oil. The oil was purified by silica chromatography, eluting with a 50-80% EtOAc/Hexane gradient, to afford (R)-ethyl 5-(2-(5-fluoro-2-methoxypyridin-3-yl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylate (0.72 g, 56.2%) as a yellow foam. MS (apci) m/z=386.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791123B2
Source datasetuspto-grants-2014_07
ORD IDord-17847951198f46e493b30f28472380b7
Source noteuspto-grants-2014_07