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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477705Generated: October 31, 2026

Dimethylformamide → HCID 117839541, compound

https://huagongshe.com/reaction/1477705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-5-nitropyridineHCID 78308—
ReactantHCID 117839396HCID 117839396—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 117839541HCID 1178395414.9%

Reaction Conditions

Temperature100 °C

Reaction Steps

An N,N-dimethylformamide suspension (1 mL) of 1-(4-chlorobenzyl)-4-(piperazin-1-yl)-1,3,5-triazin-2(1H)-one (31 mg, 0.10 mmol) synthesized in Reference Synthesis Example 9, 2-chloro-5-nitropyridine (16 mg, 0.10 mmol) and potassium carbonate (18 mg, 0.20 mmol) was stirred at 100° C. for 1 hour. After the completion of the reaction, water was added to the reaction solution and extraction with ethyl acetate from the resultant reaction solution was performed three times. The organic layer was washed with brine, was dried over anhydrous sodium sulfate, and was concentrated under reduced pressure. The resultant residue was purified by preparative silica gel thin-layer chromatography to obtain the title compound (2.1 mg, yield: 4.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403798B2
Source datasetuspto-grants-2016_08
ORD IDord-c1a1283f3a1547788cab1c5db22ec7ae
Source noteuspto-grants-2016_08