Reaktion #8741

ord-598260d8b1be4001a4fe9d3ea45a3d59

Reaktionsgleichung

BrCCCOc1cccc(-c2noc3ccsc23)c1
3-[3-(3-bromo-propoxy)-phenyl]-thieno[2,3-d]isoxazole
ClCCCOc1cccc(-c2noc3ccsc23)c1
(3-(3-chloro-propoxy)-phenyl]-thieno[2,3-d]isoxazole
NCc1ccc(F)cc1
4-fluorobenzylamine
O=C([O-])[O-].[K+].[K+]
potassium carbonate
Fc1ccc(CNCCCOc2cccc(-c3noc4ccsc34)c2)cc1
title compound
Ausbeute 94.0%
Fc1ccc(CNCCCOc2cccc(-c3noc4ccsc34)c2)cc1
(4-fluoro-benzyl)-[3-(3-thieno[2,3-d]isoxazol-3-yl-phenoxy)-propyl]-amine
Ausbeute 94.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenCombine the appropriate fractions and concentrate

Vorschrift

The title compound is prepared from a mixture of 3-[3-(3-bromo-propoxy)-phenyl]-thieno[2,3-d]isoxazole, 3-[(3-(3-chloro-propoxy)-phenyl]-thieno[2,3-d]isoxazole, 4-fluorobenzylamine and potassium carbonate essentially as described above in example 4. Combine the appropriate fractions and concentrate to give the title compound (0.36 g, 94% Yield) as an oil. Purity by LC/MS (APCI)=100% area, [M+H]+=383 m/e.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07091199B1uspto-grants-2006_08