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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81191Generated: October 29, 2026

Diisopropylethylamine → HCID 178461244, compound

https://huagongshe.com/reaction/81191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantPotassium FluorideHCID 522689—
Reactant(4aS,7aS)-octahydro-2H-cyclopenta[b]pyrazin-2-oneHCID 86724543—
ReactantHCID 178461197HCID 178461197—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
ProductHCID 178461244HCID 178461244—

Reaction Conditions

Temperature100 °C

Reaction Steps

A vial was charged with potassium fluoride (163 mg, 2.81 mmol), 2-bromo-4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-3H-imidazo[4,5-c]pyridine-6-carbonitrile (Preparative Example 3.1, 250 mg, 0.562 mmol), (4aS,7aS)-octahydro-2H-cyclopenta[b]pyrazin-2-one (189 mg, 1.349 mmol), DMSO (1730 μl) and DIEA (491 μl, 2.81 mmol). The vial was capped and heated to 100° C. overnight. The mixture was then cooled to room temperature, diluted with ethyl acetate and washed with water and brine. The organic layer was dried over magnesium sulfate, filtered, and concentrated. Purification by silica gel chromatography (0-20% MeOH in DCM) afforded 4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-2-[(4aS,7aS)-3-oxooctahydro-1H-cyclopenta[b]pyrazin-1-yl]-3H-imidazo[4,5-c]pyridine-6-carbonitrile. MS ESI calc'd. for C27H30ClN7O [M+H]+ 504. found 504.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846657B2
Source datasetuspto-grants-2014_09
ORD IDord-b13f3e42f00647aca60672636407e37a
Source noteuspto-grants-2014_09