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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 970035Erstellt: 25. Oktober 2026

Chlorosuccinimide → 4-Chloro-2-methylbenzo[d]thiazol-5-amine

https://huagongshe.com/reaction/970035

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorosuccinimideHCID 31398—
Edukt5-Benzothiazolamine, 2-methyl-HCID 36229—
LösungsmittelIsopropanolHCID 3776—
Produkt4-Chloro-2-methylbenzo[d]thiazol-5-amineHCID 11217857—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a solution of 5-amino-2-methylbenzothiazole (818 mg, 4.99 mmol) in isopropanol (12 mL) was added N-chlorosuccinimide (732 mg, 5.48 mmol). The mixture was stirred at 60° C. for 15 min., partitioned between DCM and 5% sodium bicarbonate. The organic phase was washed with brine, dried over sodium sulphate and concentrated in vacuo to give a residue that was purified with flash chromatography (EtOAc/DCM gradient elution). 4-Chloro-2-methylbenzothiazol-5-ylamine was obtained as off-white crystalline solid (510 mg, 51%). mp 121-122° C. (lit. 124° C.); TLC single spot at Rf 0.51 (20% EtOAc/DCM); 1H NMR (270 MHz, DMSO): δ 7.61 (1H, d, J=8.6 Hz, ArH), 6.91 (1H, d, J=8.6 Hz, ArH), 5.49 (2H, s, NH2), 2.75 (3H, s, CH3); APCI-MS 199 (MH)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07309715B2
Quelldatensatzuspto-grants-2007_12
ORD IDord-cc106b59f5a04d1892e6b401a20c623f
Quellennotizuspto-grants-2007_12