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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448549Generated: October 24, 2026

Ethylene Glycol → Bosentan

https://huagongshe.com/en/reaction/448549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantTolueneHCID 1140—
ReactantBarium hydroxideHCID 6093286—
Reactantp-Tert-butyl-n-[6-chloro-5-(2-methoxyphenoxy)-2-(2-pyrimidinyl)-4-pyrimidinyl]benzenesulfonamide potassium saltHCID 86650086—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductBosentanHCID 104865—

Reaction Conditions

Temperature110 °C

Reaction Steps

10 gms of p-tert-butyl-N-[6-chloro-5-(2-methoxy-phenoxy)-[2,2′-bipyrimidin]-4-yl]benzenesulfonamide potassium salt and barium hydroxide (1.5 gms) were charged to a reaction vessel. Ethylene glycol (30 ml) and toluene (150 ml) were added thereto. The reaction mass was heated at a temperature of 110° C. for 2 hours. Further 1.5 gms of barium hydroxide was added and heating was continued for another 4 hours. After completion of the reaction, toluene was removed by distillation and water (150 ml) was added. The pH of the reaction mass was adjusted to a value ranging from 1 to 2 with a mixture of 1:1 HCl:water and extracted in dichloromethane. The organic layer was collected and washed with water (150 ml) and the solvent was distilled off to obtain a residue. To the residue a mixture of ethanol and water (1:1) was added and stirred. The resulting suspension was heated to reflux to obtain a clear solution. The clear solution was further cooled to 25° C. to isolate bosentan.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481730B2
Source datasetuspto-grants-2013_07
ORD IDord-e1f3a17a4c0f465c86993396b4828e57
Source noteuspto-grants-2013_07