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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37096Generated: October 25, 2026

Sodium Glycolate → 4-tert-butyl-N-[5-(2-chloro-5methoxy-phenoxy)-6-(2-hydroxy-ethoxymethyl)-2-(morpholin-4-yl)-pyrimidin-4-yl]-benzenesulphonamide

https://huagongshe.com/reaction/37096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium GlycolateHCID 517347—
ReactantSodiumHCID 5360545—
Reactant4-tert-butyl-N-[5-(2-chloro-5-methoxy-phenoxy)-6-chloromethyl-2-(morpholin-4-yl)-pyrimidin-4-yl]-benzenesulphonamideHCID 19934755—
SolventEthylene GlycolHCID 174—
Product4-tert-butyl-N-[5-(2-chloro-5methoxy-phenoxy)-6-(2-hydroxy-ethoxymethyl)-2-(morpholin-4-yl)-pyrimidin-4-yl]-benzenesulphonamideHCID 9830283—

Reaction Conditions

Temperature80 °C

Reaction Steps

1 g of 4-tert-butyl-N-[5-(2-chloro-5-methoxy-phenoxy)-6-chloromethyl-2-(morpholin-4-yl)-pyrimidin-4-yl]-benzenesulphonamide was added to a sodium glycolate solution from 2.5 g of ethylene glycol and 0.12 g of sodium. The reaction mixture was stirred at 80° C. under argon for 72 hours. Thereafter, the ethylene glycol was distilled off and the residue was partitioned between ethyl acetate and 1 N hydrochloric acid. The organic phase was washed with water, dried over sodium sulphate and the solvent was distilled off. The residue was chromatographed over silica gel with ether. There was obtained 0.85g of 4-tert-butyl-N-[5-(2-chloro-5methoxy-phenoxy)-6-(2-hydroxy-ethoxymethyl)-2-(morpholin-4-yl)-pyrimidin-4-yl]-benzenesulphonamide. m.p 162°-164° C., MS: M=606.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05420129
Source datasetuspto-grants-1995_05
ORD IDord-8af9041743f64ffb915679f0890fb30c
Source noteuspto-grants-1995_05