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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416636Generated: October 30, 2026

Cesium carbonate → HCID 10226975, compound

https://huagongshe.com/reaction/2416636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantHCID 22632293HCID 22632293—
Reactant(2,5-Dimethoxypyrimidin-4-yl)boronic acidHCID 22632309—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventBenzeneHCID 241—
SolventDimethylformamideHCID 6228—
ProductHCID 10226975HCID 1022697513%

Reaction Conditions

Temperature80 °C

Reaction Steps

A flask was charged with N-{4-[3-(3-bromophenyl)-benzo[c]isoxazol-5-yl]-pyrimidin-2-yl}-acetamide (100 mg, 0.272 mmol), cesium carbonate (97.7 mg, 0.328 mmol), and 2,5-dimethoxypyrimidine-6-boronic acid (55.0 mg, 0.3 mmol). The flask was evacuated and back-filled with nitrogen 5-7 times before adding 5 mL of degassed p-dioxane and 1 mL of degassed DMF. To this stirring solution/suspension was added, 125 μL of a 10% w/v benzene solution of tri-tertbutylphosphine followed by the addition of Pd2(dba)3 (25 mg, 0.0272 mmol) slurred in 1 mL of degassed DMF. The reaction was stirred under nitrogen atmosphere, at 80° C. Reaction was followed by HPLC and deemed to be complete in 4 hours. The reaction mixture was suction filtered hot through a pad of diatomaceous earth and washed the precipitate with DMF and acetonitrile. The filtrate was reduced to an oil under reduced pressure and the crude material purified via HPLC utilizing acetonitrile/water/TFA as the eluent. The material was isolated as a bright yellow powder (15 mg, 13% yield). 1H NMR (500 MHz DMSO-d6) δ 8.93 (s, 1H) 8.6 (s, 1H), 8.31 (s, 1H), 8.29 (d, 1H), 8.25 (d, 1H), 8.07 (d, 1H), 7.87 (d, 1H), 7.81 (d, 1H), 7.77 (m, 1H), 4.02 (2 close sing, 6H) in ppm. LC-MS (ES+) m/e=469 (M+H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825190B2
Source datasetuspto-grants-2004_11
ORD IDord-e218a46ff184455aa014c4ab6c0e6a4f
Source noteuspto-grants-2004_11