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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1020775Erstellt: 26. Oktober 2026

Ethylene Glycol → Bosentan

https://huagongshe.com/reaction/1020775

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylene GlycolHCID 174—
EduktHydrochloric AcidHCID 313—
EduktSodium HydroxideHCID 14798—
Edukt4-Tert-butyl-n-(6-chloro-5-(2-methoxyphenoxy)-2,2'-bipyrimidin-4-yl)benzenesulfonamideHCID 11135160—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
ProduktBosentanHCID 104865—

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

Sodium hydroxide (26.66 g), ethylene glycol (400 mL), tetrabutylammonium bromide (10 g), 4-tert-butyl-N-[6-chloro-5-(2-methoxyphenoxy)-2,2′-bipyrimidin-4-yl]benzenesulfonamide (100 g) and dimethylsulphoxide (400 mL) were mixed together at 25° C. The reaction mixture was heated to 60° C. to 65° C. and the mixture was stirred for 12-14 hours at 60° C. to 65° C. The reaction mixture was cooled to 25° C. followed by the addition of dichloromethane (600 mL) and de-ionized water (1000 mL). The pH of the mixture was adjusted to 2 to 3 with concentrated hydrochloric acid and the mixture was stirred for 10 minutes. The organic layer of the reaction mixture was separated. The aqueous layer was extracted with dichloromethane (200 mL). Both the organic layers were combined, washed with de-ionized water (500 mL) and the solvent was recovered. The residue was dried under vacuum at 40° C. to 50° C. to obtain bosentan.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08716477B2
Quelldatensatzuspto-grants-2014_05
ORD IDord-8bfb742a3241403aaf99ad34d32767bb
Quellennotizuspto-grants-2014_05