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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655861Generated: October 30, 2026

1,2-Diaminocyclohexane → HCID 11996714, compound

https://huagongshe.com/reaction/655861

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DiaminocyclohexaneHCID 4610—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1H-Pyrazolo[3,4-d]pyrimidin-4-amineHCID 75420—
Reactant3-(3-Bromophenyl)-1H-pyrazoleHCID 2735613—
CatalystCopper iodideHCID 83717—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 11996714HCID 119967140.2%

Reaction Conditions

Temperature110 °C

Reaction Steps

5-(3-bromo-phenyl)-1H-pyrazole (0.3 g, 1.0 eq, 1.34 mmol) and cyclohexane-1,2-diamine (0.03 g, 0.2 eq, 0.27 mmol) were added to a pre-stirred mixture of 1H-Pyrazolo[3,4-d]pyrimidin-4-ylamine (0.22 g, 1.2 eq, 1.62 mmol), copper iodide (0.013 g, 0.5 eq, 0.68 mmol) and potassium phosphate (0.6 g, 2.1 eq, 2.84 mmol) in DMF (8 ml) under an inert atmosphere. The reaction mixture was then stirred at 110° C. for 24 hours, and allowed to cool to room temperature. Ethyl acetate (8 ml) was then added to the reaction mixture which was then filtered through a plug of silica, which was then washed with a further portion of ethylacetate (20 ml). The filtrate was concentrated to dryness in vacuo and the resultant residue was purified by column chromatography using DCM/MeOH (95:5) as eluent to yield the title compound as an off-white solid (0.9 mg, 0.0003 mmol, 0.2%). LCMS: [M+H]+=277, Rt=1.80 min, 93% purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071607B2
Source datasetuspto-grants-2011_12
ORD IDord-185a36f64512478fb6b8733d88e86fcd
Source noteuspto-grants-2011_12