Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1528218Erstellt: 26. Oktober 2026

Water → 2-tert-Butyl-6-chloro-7-(4-methylpiperazine-1-sulfonyl)-benzooxazole

https://huagongshe.com/reaction/1528218

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktTriethylamineHCID 8471—
Edukt1-MethylpiperazineHCID 53167—
Edukt2-Tert-butyl-6-chlorobenzoxazole-7-sulfonyl chlorideHCID 23447791—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-tert-Butyl-6-chloro-7-(4-methylpiperazine-1-sulfonyl)-benzooxazoleHCID 2344783698,7%

Reaktionsschritte

1.62 ml (11.68 mmol; 1.2 eq) of triethylamine followed by 1.20 ml (10.71 mmol; 1.1 eq) of 1-methylpiperazine were added to a solution of 3.0 g (9.73 mmol; 1.0 eq) of 2-tert-butyl-6-chlorobenzooxazole-7-sulfonyl chloride in 45 ml of tetrahydrofuran. The reaction medium was stirred at ambient temperature for 2 hours. Water was added and the reaction medium was extracted with ethyl acetate. The organic phases were combined, dried over magnesium sulfate, filtered and evaporated. 3.57 g of 2-tert-butyl-6-chloro-7-(4-methylpiperazine-1-sulfonyl)benzooxazole were obtained in the form of a tacky brown foam. Yield=98%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09090596B2
Quelldatensatzuspto-grants-2015_07
ORD IDord-27d4766449f9426da1785cd0a41e7c0d
Quellennotizuspto-grants-2015_07