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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287365Generated: October 30, 2026

Hydrochloric Acid → HCID 54283693, compound

https://huagongshe.com/reaction/2287365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
ReactantAcetaldehyde ammoniaHCID 522583—
ReactantSodiumHCID 5360545—
ReactantN-[6-chloro-5-(2-methoxyphenoxy)-2-(2-pyrimidinyl)-4-pyrimidinyl]-2-phenylethenesulfonamideHCID 53744388—
ProductHCID 54283693HCID 54283693—

Reaction Steps

Sodium (693 mg) was added to and dissolved in 18.2 ml of aminoethanol. To this reaction solution was added 3.00 g of N-[6-chloro-5-(2-methoxyphenoxy)-2-(2-pyrimidinyl)-4-pyrimidinyl]-2-phenylethenesulfonamide with stirring at room temperature. The reaction mixture was stirred at 60° C. for one hour and then at 80° C. for two hours followed by pouring into a mixture of 1N hydrochloric acid and ice. This solution was neutralized with a saturated sodium bicarbonate solution and extracted with ethyl acetate and the ethyl acetate layer was dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated in vacuo and the resulting residue was purified by a silica gel column chromatography (chloroform-methanol=20:1). The resulting amorphous substance was pulverized in ether and collected by filtration to give 2.40 g of N-[6-(2-hydroxyethylamino)-5-(2-methoxyphenoxy)-2-(2-pyrimidinyl)-4-pyrimidinyl]-2-phenylethenesulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06083955
Source datasetuspto-grants-2000_07
ORD IDord-2bb8aa7179674fa5ba21476e029eb2a4
Source noteuspto-grants-2000_07