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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418331Generated: October 29, 2026

Ethyl Acetate → 4-t-butyl-N-[6-(3-hydroxypropyloxy)-5-(2-methoxyphenoxy)-2-morpholino-4-pyrimidinyl]-benzenesulfonamide

https://huagongshe.com/reaction/1418331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant1,3-PropanediolHCID 10442—
ReactantSodium hydrideHCID 24758—
Reactant4-t-butyl-N-[6-chloro-5-(2-methoxyphenoxy)-2-morpholino-4-pyrimidinyl]benzenesulfonamideHCID 22729414—
SolventDimethyl SulfoxideHCID 679—
Product4-t-butyl-N-[6-(3-hydroxypropyloxy)-5-(2-methoxyphenoxy)-2-morpholino-4-pyrimidinyl]-benzenesulfonamideHCID 1538110268%

Reaction Steps

1,3-Propanediol (580 mg) was dissolved in dimethyl sulfoxide (15 ml). Sodium hydride (297 mg) and 4-t-butyl-N-[6-chloro-5-(2-methoxyphenoxy)-2-morpholino-4-pyrimidinyl]benzenesulfonamide (1.1 g) were added to the solution. The resultant mixture was stirred for 4 hours at 120° C. Ethyl acetate was added to the reaction mixture, followed by successive washing with 0.5N-HCl, water, and saturated brine. The organic layer was dried over anhydrous sodium sulfate, and evaporated. The residue was purified by silica gel column chromatography (chloroform:methanol=50:1), to thereby obtain 802 mg (yield: 68%) of the title compound as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05883092
Source datasetuspto-grants-1999_03
ORD IDord-7352672f72594bb5944891d3fb9b61ce
Source noteuspto-grants-1999_03