Reaktion #2075746

ord-b7b282921ffd4fd6892c7431aea042c0

Reaktionsgleichung

COC(=O)c1cc(O)c2cccc(SC)c2n1
quinoline
COC(=O)c1cc(O)c2cccc(SC)c2n1
2-carbomethoxy-4-hydroxy-8-methylthioquinoline
CSc1ccccc1N
2-methylmercaptoaniline
c1ccc2ncccc2c1
quinoline
COC(=O)c1cc(O)c2cccc(C)c2n1
2-carbomethoxy-4-hydroxy-8-methylquinoline
Ausbeute 59.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigewas obtained (1.24 g, 59% yield over two steps)

Vorschrift

Employing the same sequence as employed in the preparation of quinoline F3 but starting with the commercially available o-toluidene (Aldrich Chemical Co.) rather than 2-methylmercaptoaniline (F1) the desired quinoline I1 was obtained (1.24 g, 59% yield over two steps).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07642235B2uspto-grants-2010_01