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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 30899Erstellt: 24. Oktober 2026

Sulfurous Acid → N-(4-iodophenyl)-6-methyl-1,3-benzothiazol-2-amine

https://huagongshe.com/de/reaction/30899

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfurous AcidHCID 1100—
EduktAmmonium HydroxideHCID 14923—
EduktBromineHCID 24408—
EduktN-(4-iodophenyl)-N'-(4-methylphenyl)thioureaHCID 5017958—
LösungsmittelChloroformHCID 6212—
ProduktN-(4-iodophenyl)-6-methyl-1,3-benzothiazol-2-amineHCID 2198571997%

Reaktionsschritte

A suspension of N-(4-iodophenyl)-N′-(4-methylphenyl)thiourea (0.62 g, 4.68 mmol) in chloroform (23 mL) was treated with a solution of bromine (2.65 g, 16.59 mmol) in chloroform (1 mL). The reaction mixture was stirred at rt for 5 minutes and then heated at 50° C. for 5 minutes. Then the reaction mixture was allowed to cool, and was treated with sulphurous acid until the orange color disappeared. The reaction mixture was neutralized by treatment with conc. ammonium hydroxide. More chloroform was then added to dissolve the precipitate. The layers was separated, and the organic layer was washed with water and brine, dried over sodium sulfate, filtered and concentrated to give N-(4-iodophenyl)-6-methyl-1,3-benzothiazol-2-amine (0.6 g, 97%). 1H NMR (400 MHz, DMSO-d6) δ 2.36 (s, 3H), 7.12 (m, 1H), 7.48 (d, 1H), 7.60 (m, 3H), 7.65 (m, 2H), 10.50 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07423156B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-9043f7dd576c4a4bb0909f02be421dbe
Quellennotizuspto-grants-2008_09