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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466217Generated: November 2, 2026

Potassium Carbonate → HCID 71539682, compound

https://huagongshe.com/reaction/1466217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,2-Diaminocyclohexane, trans-HCID 43806—
ReactantHCID 71539791HCID 71539791—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 71539682HCID 71539682—

Reaction Conditions

Temperature100 °C

Reaction Steps

5-(((3,5-Bis(trifluoromethyl)benzyl)(5-bromopyrimidin-2-yl)amino)methyl)-1-(tert-butyl)-N,N-bis(cyclopropylmethyl)-3-methyl-1H-pyrazolo[3,4-b]pyridin-6-amine (0.2 g, 0.293 mmol), obtained in step (vi) of Example 1,2-pyrrolidinone (0.024 g, 0.293 mmol), CuI (0.005 mg, 0.029 mmol), trans-1,2-diaminocyclohexane (0.007 g, 0.064 mmol) were taken in a sealed tube in 1,4-dioxane (5 mL), which was degassed with argon for 15 min. K2CO3 (0.08 g, 0.586 mmol) was added to it. The reaction mixture was stirred at 100° C. for 28 h. Thereafter the reaction mixture was filtered through celite, extracted with EtOAc. The combined organic layer was washed with water, dried over Na2SO4, concentrated under reduced pressure, and purified by column chromatography using EtOAc-petroleum ether as eluent to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000007B2
Source datasetuspto-grants-2015_04
ORD IDord-38d001ee03b6433db5aa912ec43084a2
Source noteuspto-grants-2015_04