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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889500Generated: November 3, 2026

Bromoacetone → HCID 136052257, compound

https://huagongshe.com/reaction/1889500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetoneHCID 11715—
ReactantHydroxylamine HClHCID 21645—
ReactantSodium hydrideHCID 24758—
ReactantSodium BicarbonateHCID 516892—
Reactant4'-[(6-ethyl-2,4-dioxo-3,4-dihydrothieno[2,3-d]pyrimidin-1(2H)-yl)methyl]biphenyl-2-carbonitrileHCID 59351770—
SolventDimethyl SulfoxideHCID 679—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
ProductHCID 136052257HCID 13605225712%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a mixture of 4′-[(6-ethyl-2,4-dioxo-3,4-dihydrothieno[2,3-d]pyrimidin-1(2H)-yl)methyl]biphenyl-2-carbonitrile (1 g), 1-bromoacetone (0.26 mL) and N,N-dimethylformamide (20 mL) was added sodium hydride (0.15 g), and the mixture was stirred at 50° C. for 3 hr. The reaction mixture was diluted with chloroform, 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 residue obtained by silica gel column chromatography was dissolved in dimethyl sulfoxide (5 mL), and the mixture was added to a mixture of hydroxylammonium chloride (1.88 g), sodium hydrogencarbonate (2.84 g) and dimethyl sulfoxide (20 ml,), which had been stirred at 40° C. for 30 min in advance. The reaction mixture was stirred at 90° C. for 16 hr, diluted with chloroform, washed successively with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent-was evaporated under reduced pressure. The residue was purified by silica gel column chromatography and dissolved in methylene chloride (30 mL). N,N′-Carbonyldiimidazole (0.27 g) and then 1,8-diazabicyclo[5.4.0]undec-7-ene (0.23 mL) were added, and the mixture was stirred at room temperature for 2 hr. The reaction mixture was diluted with chloroform, washed successively with saturated aqueous potassium hydrogensulfate solution and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was dissolved in methylene chloride (50 mL), iodine acid (0.73 g) was added, and the mixture was stirred at room temperature for 24 hr. The reaction mixture was washed successively with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by preparative HPLC to give the title compound as colorless crystals (0.15 g, 12%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501750B2
Source datasetuspto-grants-2013_08
ORD IDord-069cc80d6b8e4b0b94a4af3ac2fb298c
Source noteuspto-grants-2013_08