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HRID 1020775作成日:2026年10月27日

Ethylene Glycol → Bosentan

https://huagongshe.com/reaction/1020775

反応式

関与物質

役割名称HCID仕込み量
反応物Ethylene GlycolHCID 174—
反応物Hydrochloric AcidHCID 313—
反応物Sodium HydroxideHCID 14798—
反応物4-Tert-butyl-n-(6-chloro-5-(2-methoxyphenoxy)-2,2'-bipyrimidin-4-yl)benzenesulfonamideHCID 11135160—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物BosentanHCID 104865—

反応条件

温度25 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08716477B2
出典データセットuspto-grants-2014_05
ORD IDord-8bfb742a3241403aaf99ad34d32767bb
出典メモuspto-grants-2014_05