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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326708Generated: October 24, 2026

Sodium Glycolate → N-[6-(2-hydroxy-ethoxy)-5-(p-methoxyphenyl)-4-pyrimidinyl]-p-toluenesulfon-amide

https://huagongshe.com/en/reaction/326708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium GlycolateHCID 517347—
ReactantSodiumHCID 5360545—
ReactantN-[6-chloro-5-(p-methoxyphenyl)-4-pyrimidinyl]-p-toluenesulfonamideHCID 19735459—
SolventEthylene GlycolHCID 174—
ProductN-[6-(2-hydroxy-ethoxy)-5-(p-methoxyphenyl)-4-pyrimidinyl]-p-toluenesulfon-amideHCID 19735450—

Reaction Steps

190 mg of N-[6-chloro-5-(p-methoxyphenyl)-4-pyrimidinyl]-p-toluenesulfonamide were added to a sodium glycolate solution from 46 mg of sodium in 1 ml of ethylene glycol. After a reaction period of 5 hours at 100° C., the reaction mixture was evaporated to dryness under reduced pressure. The residue was partitioned between ethyl acetate and 1N hydrochloric acid. The organic phase was washed neutral, dried and evaporated under reduced pressure. The residue was chromatographed on silica gel with methylene chloride and ethyl acetate (4:1 v/v). There were obtained 175 mg of N-[6-(2-hydroxy-ethoxy)-5-(p-methoxyphenyl)-4-pyrimidinyl]-p-toluenesulfon-amide, melting point 147°-149° C. (from methylene chloride/hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05270313
Source datasetuspto-grants-1993_12
ORD IDord-e2b486f0faba44978e09600883630e9b
Source noteuspto-grants-1993_12