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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452584Generated: October 30, 2026

Tetramethyltin → 4-(2-Methoxyethoxy)-2-(6-methylpyridin-3-yl)-6-(pyrazolo[1,5-a]pyridin-3-ylcarbonyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine

https://huagongshe.com/reaction/452584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetramethyltinHCID 11661—
Reactant[2-(6-Chloropyridin-3-yl)-4-(2-methoxyethoxy)-7,8-dihydropyrido[4,3-d]pyrimidin-6(5h)-yl](pyrazolo[1,5-a]pyridin-3-yl)methanoneHCID 49821989—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product4-(2-Methoxyethoxy)-2-(6-methylpyridin-3-yl)-6-(pyrazolo[1,5-a]pyridin-3-ylcarbonyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidineHCID 4982207349%

Reaction Conditions

Temperature150 °C

Reaction Steps

To a solution of 30 mg (0.065 mmol) O-2 in 1 mL DMF in a microwave vial was added approximately 20 uL (˜0.15 mmol) tetramethyltin and 8 mg (˜10 mol %) tetrakistriphenylphosphinepalladium(0). The reaction was heated by microwave irradiation for 20 minutes at 150° C. After cooling, the reaction was purified by reverse phase HPLC (CH3CN/H2O with TFA as modifier), and the fractions containing the product were partitioned between EtOAc and saturated aqueous NaHCO3. The organic layer was washed with brine, dried over Na2SO4, filtered and concentrated to provide R-1 as a white solid (14 mg, 49% yield). HRMS m/z (M+H) 445.1977 found, 445.1983 required.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492392B2
Source datasetuspto-grants-2013_07
ORD IDord-f67e3aa8cdcc486596c9da51813412aa
Source noteuspto-grants-2013_07