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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799467Generated: October 31, 2026

Pyridine → HCID 25106899, compound

https://huagongshe.com/reaction/1799467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant(3-Acetamidophenyl)boronic acidHCID 157274—
ReactantHCID 68701666HCID 68701666—
CatalystCupric acetateHCID 8895—
SolventDimethylformamideHCID 6228—
SolventSodium BicarbonateHCID 516892—
ProductHCID 25106899HCID 2510689964.6%

Reaction Conditions

Temperature65 °C

Reaction Steps

According to Scheme 4 Step 2: A mixture of compound 8(A) (100 mg, 0.39 mmol), 3-acetamidophenylboronic acid (107 mg, 0.59 mmol), copper acetate (79 mg, 0.44 mmol) and pyridine (65 μl, 0.79 mmol) in DMF (3 mL) was stirred at 65° C. during 15 hours. The reaction mixture was diluted with 100 mL of a saturated solution of NaHCO3 and the aqueous layer was extracted twice with DCM (100 mL). The organic layers were combined and successively dried over MgSO4, filtered 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 20 g, C18) using Water/CH3CN 6/4 as eluant to afford N-(3-(4-(4-chlorobenzyl)-6-methyl-3,5-dioxo-4,5-dihydro-1,2,4-triazin-2(3H)-yl)phenyl)acetamide 8(B) (97 mg, 63%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344138B2
Source datasetuspto-grants-2013_01
ORD IDord-214d58ff31f1494b9f6ffb92e8a18a51
Source noteuspto-grants-2013_01