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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1020775생성일: 2026년 10월 26일

Ethylene Glycol → Bosentan

https://huagongshe.com/reaction/1020775

반응식

참여 물질

역할이름HCID투입량
반응물Ethylene GlycolHCID 174—
반응물Hydrochloric AcidHCID 313—
반응물Sodium HydroxideHCID 14798—
반응물4-Tert-butyl-n-(6-chloro-5-(2-methoxyphenoxy)-2,2'-bipyrimidin-4-yl)benzenesulfonamideHCID 11135160—
촉매Tetrabutylammonium BromideHCID 74236—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물BosentanHCID 104865—

반응 조건

온도25 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08716477B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-8bfb742a3241403aaf99ad34d32767bb
출처 메모uspto-grants-2014_05