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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799462Generated: October 31, 2026

Pyridine → HCID 68701529, compound

https://huagongshe.com/reaction/1799462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant(3-Acetamidophenyl)boronic acidHCID 157274—
ReactantHCID 68702647HCID 68702647—
CatalystCupric acetateHCID 8895—
SolventDimethylformamideHCID 6228—
SolventSodium BicarbonateHCID 516892—
ProductHCID 68701529HCID 6870152946.2%

Reaction Conditions

Temperature65 °C

Reaction Steps

According to Scheme 3 Step 2: A mixture of compound 6(A) (1.10 g, 4.74 mmol), 3-acetamidophenylboronic acid (1.20 g, 6.64 mmol), copper acetate (258 mg, 1.42 mmol) and pyridine (229 μL, 2.84 mmol) in DMF (30 mL) was stirred at 65° C. during 15 h under room atmosphere. The mixture was diluted with 50 mL of a saturated solution of NaHCO3 and the aqueous layer was extracted twice with 60 mL of DCM. The organic layers were combined dried over MgSO4, filtered filtrated and concentrated under reduce pressure to afford a brown solid. The crude solid was purified by flash chromatography with silica gel (Merck Flashmart prepacked column 10 g SiO2) (Eluant: CH2Cl2/MeOH 98/2) to afford N-(3-(4-allyl-6-bromo-3,5-dioxo-4,5-dihydro-1,2,4-triazin-2(3H)-yl)phenyl)acetamide 6(B) (800 mg, 46%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344138B2
Source datasetuspto-grants-2013_01
ORD IDord-df4887005dc347538e977a8830ee8b41
Source noteuspto-grants-2013_01