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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1917088Generated: October 31, 2026

Triphenylphosphine → 6-bromo-4-methyl-2-(2-thiophen-2-yl-ethyl)-2H-[1,2,4]triazine-3,5-dione

https://huagongshe.com/reaction/1917088

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-ThiopheneethanolHCID 79400—
Reactant6-bromo-4-methyl-1,2,4-triazine-3,5(2h,4h)-dioneHCID 260564—
ReactantDiethyl azodicarboxylateHCID 5462977—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product6-bromo-4-methyl-2-(2-thiophen-2-yl-ethyl)-2H-[1,2,4]triazine-3,5-dioneHCID 5826980379%

Reaction Conditions

Temperature70 °C

Reaction Steps

0.4 g (1.94 mmol) of intermediate 2a are placed in the presence of 0.24 mL (2.14 mmol) of 2-thiophen-2-yl-ethanol, 0.61 g (2.33 mmol) of triphenylphosphine in 4 mL of THF. At 0° C., 0.54 mL (2.33 mmol) of DEAD in solution in toluene are added dropwise. The reaction medium is heated for 7 h at 70° C. After concentration, the obtained residue is taken up with ethyl acetate and washed with water. After drying on MgSO4, the organic phase is dry concentrated. The obtained residue is purified by flash chromatography on silica (CH2Cl2/MeOH, gradient 100/0 to 97/3 over 30 min). 0.48 g of crystals corresponding to the compound 4k are obtained (yield: 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618287B2
Source datasetuspto-grants-2013_12
ORD IDord-d8930fc73b854711bb04d529f1351cbd
Source noteuspto-grants-2013_12