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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2287363Generated: October 25, 2026

Hydrochloric Acid → HCID 53705989, compound

https://huagongshe.com/reaction/2287363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodiumHCID 5360545—
ReactantN-[6-chloro-5-(2-methoxyphenoxy)-2-(2-pyrimidinyl)-4-pyrimidinyl]-2-phenylethenesulfonamideHCID 53744388—
SolventIsopropanolHCID 3776—
ProductHCID 53705989HCID 5370598927.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

Sodium (181 mg) was added to 10 ml of isopropyl alcohol and, after one hour, 100 ml of isopropyl alcohol was added thereto followed by heating at 60° C. to dissolve. To this reaction solution was added 400 mg 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 room temperature for 1.25 hours and then at 60° C. for 45 minutes followed by pouring into a mixture of 1N hydrochloric acid and ice. The solution was extracted with chloroform and the chloroform layer was dried over anhydrous magnesium sulfate followed by filtering. The filtrate was concentrated in vacuo and the resulting residue was purified by a silica gel column chromatography (ethyl acetate). The resulting amorphous substance was crystallized in ether and collected by filtration to give 57 mg of N-[6-isopropoxy-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-452d272f4d7b45f9b96b6ba4756daccd
Source noteuspto-grants-2000_07