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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2427239Erstellt: 25. Oktober 2026

Hydrochloric Acid → 2,4-Dichloro-N-[3,5-dichloro-4-(6-chloro-benzothiazol-2-yloxy)-phenyl]benzenesulfonamide

https://huagongshe.com/reaction/2427239

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktWaterHCID 962—
EduktBenzenesulfonyl chloride, 2,4-dichloro-HCID 204419—
Edukt3,5-Dichloro-4-(6-chloro-benzothiazol-2-yloxy)-phenylamineHCID 22148776—
LösungsmittelPyridineHCID 1049—
Produkt2,4-Dichloro-N-[3,5-dichloro-4-(6-chloro-benzothiazol-2-yloxy)-phenyl]benzenesulfonamideHCID 1020958646,4%

Reaktionsschritte

A solution of 3,5-dichloro-4-(6-chloro-benzothiazol-2-yloxy) -phenylamine (364) (2.0 g, 5.79 mmol) and 2,4-dichloro benzenesulfonylchloride (1.5 g, 6.08 mmol) in pyridine (10 ml) was stirred at room temperature for 12-hr. Water was added to the reaction mixture, which was then acidified by 2N HCl. Reaction mixture was extracted twice with AcOEt. Organic layer was washed by Brine, dried over MgSO4 and concentrated. Crude residue was purified by column chromatography (H/A=4/1, 80 g of silica gel) to afford title compound (366) (1.49 g, 46%) as a white solid. mp 73-75° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07968567B2
Quelldatensatzuspto-grants-2011_06
ORD IDord-65723c2c1beb415fa873495b991a8f29
Quellennotizuspto-grants-2011_06