Reaktion #9222

ord-507cd915806547c7b328f3dffb50e852

Reaktionsgleichung

Nc1nc2ccc(Cc3ccccc3)cc2s1
2-amino-6-benzyl-benzothiazole
CCN(CC)CC
triethylamine
CCN=C=O
ethyl isocyanate
CCNC(=O)Nc1nc2ccc(Cc3ccccc3)cc2s1
desired compound
Ausbeute 56.0%
CCNC(=O)Nc1nc2ccc(Cc3ccccc3)cc2s1
1-(6-Benzyl-2-benzothiazolyl)-3-ethylurea
Ausbeute 56.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
95°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

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

Vorschrift

A suspension of 2-amino-6-benzyl-benzothiazole (0.040 g, 0.17 mmol), triethylamine (0.104 mL, 0.77 mmol, 4.5 eq), and ethyl isocyanate (0.049 mL, 0.64 mmol, 3.8 eq) in 1 mL toluene was heated at about 95° C. for about 16 hours. The precipitate was filtered off, washed with Et2O and MeOH, and dried under vacuum to give the desired compound 0.029 g (56%). LC/MS 312.3 (M+1); LC retention time 2.62 min.

Quelle

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