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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590793Generated: October 30, 2026

Potassium Carbonate → 6-chloro-N-methyl-1-trityl-1H-pyrazolo[4,3-c]pyridin-3-amine

https://huagongshe.com/reaction/590793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium HydroxideHCID 14923—
ReactantL-ProlineHCID 145742—
ReactantMethylamine hydrochlorideHCID 6364545—
Reactant6-Chloro-3-iodo-1-trityl-1H-pyrazolo[4,3-c]pyridineHCID 89525858—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
Product6-chloro-N-methyl-1-trityl-1H-pyrazolo[4,3-c]pyridin-3-amineHCID 118272406—

Reaction Steps

6-Chloro-3-iodo-1-trityl-1H-pyrazolo[4,3-c]pyridine (Intermediate 1C; 6.08 g, 11.65 mmol), proline (0.42 g, 3.65 mmol), copper(I) iodide (0.24 g, 1.260 mmol), potassium carbonate (9.83 g, 71.1 mmol), and methylamine hydrochloride (3.26 g, 48.3 mmol) were stirred in DMSO (45 mL) at 70° C. for 24 h. Room temperature was attained, ammonium hydroxide was added, and the products extracted into DCM (×2). The combined organic extracts were washed with brine, dried over MgSO4, filtered, and concentrated in vacuo. Purification of the residue by flash chromatography (6-50% EtOAc-hexanes) gave 6-chloro-N-methyl-1-trityl-1H-pyrazolo[4,3-c]pyridin-3-amine MS ESI calc'd. For C26H21ClN4 [M+1]+ 425. found 425.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233979B2
Source datasetuspto-grants-2016_01
ORD IDord-48ce9db52e794b63a99f20805e6b577c
Source noteuspto-grants-2016_01