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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590796Generated: October 30, 2026

Ethylamine hydrochloride → 6-chloro-N-ethyl-1-trityl-1H-pyrazolo[4,3-c]pyridin-3-amine

https://huagongshe.com/reaction/590796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamine hydrochlorideHCID 11198—
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium HydroxideHCID 14923—
ReactantL-ProlineHCID 145742—
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-ethyl-1-trityl-1H-pyrazolo[4,3-c]pyridin-3-amineHCID 118272006—

Reaction Steps

6-Chloro-3-iodo-1-trityl-1H-pyrazolo[4,3-c]pyridine (Intermediate 1C; 5.53 g, 10.60 mmol), proline (0.42 g, 3.65 mmol), copper (I) iodide (0.21 g, 1.103 mmol), potassium carbonate (7.40 g, 53.5 mmol), and ethylamine hydrochloride (2.78 g, 34.1 mmol) were stirred in DMSO (30 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-ethyl-1-trityl-1H-pyrazolo[4,3-c]pyridin-3-amine. MS ESI calc'd. For C27H23ClN4 [M+1]+ 439. found 439.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233979B2
Source datasetuspto-grants-2016_01
ORD IDord-b340ca210ebb4a15b375539f5f879250
Source noteuspto-grants-2016_01