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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588087Generated: October 30, 2026

Methyl iodide → 6-chloro-3-methoxy-4-methyl-1-trityl-1H-pyrazolo[4,3-c]pyridine

https://huagongshe.com/reaction/588087

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant6-chloro-4-methyl-1-trityl-1H-pyrazolo[4,3-c]pyridin-3(2H)-oneHCID 118272136—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product6-chloro-3-methoxy-4-methyl-1-trityl-1H-pyrazolo[4,3-c]pyridineHCID 118272149—

Reaction Steps

A solution of 6-chloro-4-methyl-1-trityl-1H-pyrazolo[4,3-c]pyridin-3(2H)-one (Intermediate 4B; 406 mg, 0.953 mmol) in DMF (3 mL) was charged with potassium carbonate (348 mg, 2.52 mmol) and methyl iodide (0.089 mL, 1.430 mmol) and stirred at room temperature for 1 h. The reaction mixture was diluted with water, filtered, and dried under vacuum to give 6-chloro-3-methoxy-4-methyl-1-trityl-1H-pyrazolo[4,3-c]pyridine, which was carried onto the next step without further purification. MS ESI calc'd. for C27H22ClN3O [M+1]+ 440. found 440.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226922B2
Source datasetuspto-grants-2016_01
ORD IDord-d78f7bdde08e4323bfbaa895c16dc85f
Source noteuspto-grants-2016_01