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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889455Generated: October 30, 2026

Dimethylformamide → HCID 136052295, compound

https://huagongshe.com/reaction/1889455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 15290996HCID 15290996—
ReactantHCID 59351824HCID 59351824—
SolventEthyl AcetateHCID 8857—
ProductHCID 136052295HCID 13605229546%

Reaction Steps

A mixture of 5-methyl-3-(2-phenylethyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione (1.5 g), 3-[4′-(bromomethyl)biphenyl-2-yl]-5-(trichloromethyl)-1,2,4-oxadiazole (2.49 g), potassium carbonate (0.8 g) and N,N-dimethylformamide (30 mL) was stirred at room temperature for 2 hr. The reaction mixture was diluted with ethyl acetate, washed successively with 5% aqueous potassium hydrogensulfate solution and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography and dissolved in tetrahydrofuran (15 mL) and methanol (15 mL). 1N Aqueous sodium hydroxide solution (15 mL) was added, and the mixture was stirred at room temperature for 2 hr. The reaction mixture was adjusted to pH 4 with water and 1N hydrochloric acid, and the mixture was extracted with ethyl acetate. The obtained ethyl acetate layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound as colorless crystals (1.27 g, 46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501750B2
Source datasetuspto-grants-2013_08
ORD IDord-5685139fe6854041b7256f923140b74d
Source noteuspto-grants-2013_08