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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588175Generated: October 29, 2026

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

https://huagongshe.com/reaction/588175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant6-chloro-1-trityl-1H-pyrazolo[4,3-c]pyridin-3(2H)-oneHCID 118272301—
SolventDimethylformamideHCID 6228—
Product6-chloro-3-methoxy-1-trityl-1H-pyrazolo[4,3-c]pyridineHCID 118271897—

Reaction Steps

6-Chloro-1-trityl-1H-pyrazolo[4,3-c]pyridin-3(2H)-one (Intermediate 3B; 194 mg, 0.471 mmol), K2CO3 (132 mg, 0.955 mmol), and iodomethane (0.044 mL, 0.707 mmol) were stirred in DMF (5 mL) at room temperature for 2 h. Water was added and the products extracted into EtOAc (×2). The combined organic extracts were washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. The residue was triturated in MeOH to give 6-chloro-3-methoxy-1-trityl-1H-pyrazolo[4,3-c]pyridine, which was carried onto the next step without further purification. MS ESI calc'd. For C26H20ClN3O [M+1]+ 426. found 426.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226922B2
Source datasetuspto-grants-2016_01
ORD IDord-2b6b1e1196a84d4ba1a50f9c249d8dea
Source noteuspto-grants-2016_01