Reaktion #9224

ord-b5f2f4212b8240a4b4901953e91f7565

Reaktionsgleichung

Nc1nc2ccc(Br)cc2s1
2-amino-6-bromo-benzothiazole
CCN(CC)CC
triethylamine
CCN=C=O
ethyl isocyanate
CCNC(=O)Nc1nc2ccc(Br)cc2s1
desired compound
Ausbeute 94.0%
CCNC(=O)Nc1nc2ccc(Br)cc2s1
1-(6-Bromo-2-benzothiazolyl)-3-ethylurea
Ausbeute 94.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
90°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe precipitate was filtered off
  2. 2
    Waschenwashed with Et2O
  3. 3
    Sonstigedried under vacuum

Vorschrift

A suspension of 2-amino-6-bromo-benzothiazole (6.12 g, 26.2 mmol), triethylamine (7.30 mL, 52.4 mmol, 2.0 eq), and ethyl isocyanate (4.15 mL, 52.4 mmol, 2.0 eq) in 50 mL toluene was heated at about 90° C. for about 15 hours. The precipitate was filtered off, washed with Et2O, and dried under vacuum to give the desired compound 7.39 g (94%). LC/MS 300.0 (M−1); LC retention time 3.01 min.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07091227B2uspto-grants-2006_08