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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581814Generated: November 1, 2026

1,4-Bis(diphenylphosphino)butane → 2-(3-Thienyl)-6-methyl-4-(1-methyl-3-trifluoromethyl-5-pyrazolyloxy)-pyrimidine

https://huagongshe.com/reaction/581814

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Bis(diphenylphosphino)butaneHCID 82124—
ReactantSodium BicarbonateHCID 516892—
ReactantThiophene-3-boronic acidHCID 581760—
Reactant2-Chloro-6-methyl-4-(1-methyl-3-trifluoromethyl-5-pyrazolyloxy)pyrimidineHCID 53771522—
CatalystBis(benzonitrile)palladium chlorideHCID 498840—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Solvent1,4-DioxaneHCID 31275—
Product2-(3-Thienyl)-6-methyl-4-(1-methyl-3-trifluoromethyl-5-pyrazolyloxy)-pyrimidineHCID 5412631786%

Reaction Steps

0.145 g of 1,4-bis(diphenylphosphino)butane and 0.115 g bis(benzonitrile)palladium(II)chloride are refluxed in 10 m toluene under nitrogen for 2 hours. At room temperature 1 g 2-chloro-6-methyl-4-(1-methyl-3-trifluoromethyl-5-pyrazolyloxy)pyrimidine, 0.55 g thiophene-3-boronic acid, 0.8 g sodium hydrogen carbonate, 15 mL water and 20 mL dioxane are added, and the mixture is heated to reflux. After 2 hours another 0.2 g thiophene-3-boronic acid are added, and reflux continued for 1 hour. The organic phase is washed with with water and chromatographed to give 1 g of the title compound (m.p. 122° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05922726
Source datasetuspto-grants-1999_07
ORD IDord-93cb220babf04760a7f6172c777ddb8a
Source noteuspto-grants-1999_07