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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571383Generated: October 25, 2026

Ethyl Acetate → 6-chloro-3-(methoxymethyl)-1-trityl-1H-pyrazolo[4,3-c]pyridine

https://huagongshe.com/reaction/571383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantCesium carbonateHCID 10796—
ReactantPotassium trifluoro(methoxymethyl)borate(1-)HCID 45588148—
Reactant6-Chloro-3-iodo-1-trityl-1H-pyrazolo[4,3-c]pyridineHCID 89525858—
CatalystAllyl(1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene)chloropalladium(II)HCID 105144—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product6-chloro-3-(methoxymethyl)-1-trityl-1H-pyrazolo[4,3-c]pyridineHCID 89526490—

Reaction Conditions

Temperature100 °C

Reaction Steps

Under Argon, the solution of 6-chloro-3-iodo-1-trityl-1H-pyrazolo[4,3-c]pyridine (52 mg, 0.100 mmol), potassium methoxymethyltrifluoroborate (16.66 mg, 0.110 mmol), palladium(II) acetate (0.671 mg, 2.99 μmol), (2-DICYCLOHEXYLPHOSPHINO-2′,6′-DIISOPROPYL-1,1′-BIPHENYL)[2-(2-AMINOETHYL)PHENYL)]PALLADIUM(II) (4.36 mg, 5.98 μmol and cesium carbonate (0.024 ml, 0.299 mmol) in 1,4-Dioxane (0.9 ml) and Water (0.1 ml) was allowed to stir at 100° C. for 24 h. LC-MS showed the desired product's mass. EtOAc was added into the mixture and the organic layer was washed by water and brine. After drying over Na2SO4 the organic layer was evaporated under reduced pressure yielding 6-chloro-3-(methoxymethyl)-1-trityl-1H-pyrazolo[4,3-c]pyridine, 52a. The intermediate was taken to the next reaction without further purification. MS ESI Calc'd for C27H22ClN3O [M+H]+ 440, found 440.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023865B2
Source datasetuspto-grants-2015_05
ORD IDord-0ecdedde8bb748fdbddddd7a0aae9312
Source noteuspto-grants-2015_05