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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1797071Generated: November 4, 2026

HCID 21948669, compound → HCID 10298190, compound

https://huagongshe.com/reaction/1797071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21948669HCID 21948669—
ReactantHCID 178477796HCID 178477796—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10298190HCID 1029819045.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of ethyl 7-chloro-3-[2-(cyclopentylamino)-4-pyrimidinyl]-2-(4-fluorophenyl)pyrazolo[1,5-a]pyridine-6-carboxylate (90 mg, 0.19 mmol) in tetrahydrofuran (1 mL) was added dimethylzinc (281 μL, 2.0 M in toluene, 0.56 mmol) and tetrakis(triphenylphosphine)palladium (21 mg, 0.018 mmol). The reaction mixture was stirred at 60° C. for 16 hours. The reaction mixture was quenched with ice water then extracted with ethyl acetate. The organic layer was washed with water and brine, then dried over magnesium sulfate. Filtration and concentration, followed by flash chromatography (49:1 dichloromethane:methanol) provided ethyl 3-[2-(cyclopentylamino)-4-pyrimidinyl]-2-(4-fluorophenyl)-7-methylpyrazolo[1,5-a]pyridine-6-carboxylate (40 mg, 45%). 1H NMR (300 MHz, CDCl3) δ 8.34 (d, 1H), 8.11 (d, 1H), 7.91 (d, 1H), 7.70 (m, 2H), 7.19 (t, 2H), 6.36 (d, 1H), 5.33 (br, 1H), 4.47 (q, 2H), 4.38 (m, 1H), 3.26 (s, 3H), 2.12 (m, 2H), 1.83–1.43 (m, 9H); MS m/z 460 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07034030B2
Source datasetuspto-grants-2006_04
ORD IDord-33c6a4ed173e4e8ea787178e126714ca
Source noteuspto-grants-2006_04