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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403563Generated: October 31, 2026

Hydrochloric Acid → HCID 58467975, compound

https://huagongshe.com/reaction/2403563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium ChlorideHCID 5234—
ReactantSodium hydrideHCID 24758—
Reactant4-(Methylsulfonyl)anilineHCID 79617—
Reactant3,3,3-Trifluoro-1-propanolHCID 137512—
ReactantSodium BicarbonateHCID 516892—
Reactant2,4-Dichloro-5-(trifluoromethyl)pyrimidineHCID 2782774—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 58467975HCID 58467975—

Reaction Steps

A solution of 1.00 g (4.63 mmol) of 2,4-dichloro-5-trifluoromethylpyrimidine and 0.68 g (5.99 mmol) of 3,3,3-trifluoro-1-propanol in 12.2 ml of diethyl ether and 12.2 ml of acetonitrile was admixed at 0° C. with stirring in portions with 0.24 g of sodium hydride (55%). The mixture was slowly warmed to room temperature overnight in an ice bath. The mixture was admixed with ice and dilute sodium chloride solution. Extraction was carried out with ethyl acetate (2×). The combined organic phases were dried (Na2SO4), filtered and concentrated by evaporation. This gave 1.50 g of the crude product. 1.03 g of the crude product and 0.59 g (3.48 mmol) of 4-methanesulphonylphenylamine in 24.1 ml of acetonitrile were admixed with 0.87 ml of a 4N solution of hydrogen chloride in dioxane and stirred for 24 hours at 60° C. The mixture was admixed with a small amount of sodium hydrogen carbonate solution and concentrated in a rotary evaporator. The resulting residue was purified by means of HPLC. This gave 0.07 g (0.15 mmol) of the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802686B2
Source datasetuspto-grants-2014_08
ORD IDord-69e3c088e93a449b9dd1d92f6d8c9219
Source noteuspto-grants-2014_08