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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198094Generated: October 30, 2026

N,N'-Dimethylethylenediamine → 1-(4-Fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carboxylic acid (6-methanesulfonyl-pyridin-3-ylmethyl)-amide

https://huagongshe.com/reaction/2198094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N'-DimethylethylenediamineHCID 8070—
ReactantEthyl AcetateHCID 8857—
ReactantSodium methanesulfinateHCID 2733271—
ReactantHCID 45138009HCID 45138009—
Catalystcopper(II) trifluoromethanesulfonateHCID 2734996—
SolventDimethyl SulfoxideHCID 679—
SolventAmmonium ChlorideHCID 25517—
Product1-(4-Fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carboxylic acid (6-methanesulfonyl-pyridin-3-ylmethyl)-amideHCID 45138010—

Reaction Conditions

Temperature110 °C

Reaction Steps

To a microwave tube charged with 1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carboxylic acid (6-bromopyridin-3-ylmethyl)-amide (62 mg, 0.15 mmol) in DMSO (1 mL) was added copper (II) trifluoromethanesulfonate (53 mg, 0.15 mmol), sodium methanesulfinate (24 mg, 0.24 mmol) and N,N′ dimethylethylene diamine (47 μL, 0.44 mmol). The mixture was warmed at 110° C. for 45 minutes in the microwave. The reaction was monitored by TLC (EtOAc). The reaction was the diluted with saturated aqueous ammonium chloride (10 mL) and extracted with EtOAc (4×7 mL). The combined organic layers were washed with saturated aqueous ammonium chloride (3×7 mL), brine (7 mL), aqueous K2CO3 (7 mL), brine (7 mL), dried over magnesium sulfate, filtered and concentrated. The solid was triturated with ether to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338610B2
Source datasetuspto-grants-2012_12
ORD IDord-badfeb6fd5c24bc79935b5f7bb59dabd
Source noteuspto-grants-2012_12