HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 970035Erstellt: 24. Oktober 2026
Chlorosuccinimide → 4-Chloro-2-methylbenzo[d]thiazol-5-amine
https://huagongshe.com/de/reaction/970035
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Chlorosuccinimide | HCID 31398 | — |
| Edukt | 5-Benzothiazolamine, 2-methyl- | HCID 36229 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Produkt | 4-Chloro-2-methylbenzo[d]thiazol-5-amine | HCID 11217857 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07309715B2 |
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| Quelldatensatz | uspto-grants-2007_12 |
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| ORD ID | ord-cc106b59f5a04d1892e6b401a20c623f |
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| Quellennotiz | uspto-grants-2007_12 |
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