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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392116Generated: November 1, 2026

Acetonitrile → HCID 10134293, compound

https://huagongshe.com/reaction/1392116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantTriethylamineHCID 8471—
Reactant3,4-Dimethoxyphenylboronic acidHCID 2734702—
ReactantHCID 68524877HCID 68524877—
CatalystCupric acetateHCID 8895—
SolventEthyl AcetateHCID 8857—
ProductHCID 10134293HCID 1013429310.4%

Reaction Conditions

Temperature52.5 °C

Reaction Steps

A mixture of 6-cyclopropylamino-2-trifluoromethyladenine (46 mg, 0.2 mmol), 3,4-dimethoxyphenyl boronic acid (44 mg, 0.24 mmol), copper(II) acetate (36 mg, 0.2 mmol), triethylamine (1.0 mmol, 101 mg), anhydrous acetonitrile (4 ml) and molecular seives (˜10 pellets) was stirred at 50-55° C. for 18 hours. Ethyl acetate (20 ml) was added and the solid was removed by filtration. The filtrate was washed with 20 ml of 5% sodium bicarbonate aqueous solution. Evaporation and chromatography over SiO2 using hexane/ethylacetate/methanol (50:50:1) as elunt gave 7.9 mg of the title compound (yield 10%). 1H NMR (300 MHz, CDCl3) δ 8.10 (s, 1H), 7.39 (s, 1H), 7.13 (d, J=8.7 Hz, 2H), 6.98 (d, J=8.7 Hz, 2H), 6.35(b, 1H), 3.93 (s, 3H), 3.90 (s, 3H), 3.18 (b, 1H), 0.91 (m, 2H), 0.69 (m, 2H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07342021B2
Source datasetuspto-grants-2008_03
ORD IDord-63b80953e212489c8ffb401f1c5763f9
Source noteuspto-grants-2008_03