Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

136343-79-8

N-(2-Chlorophenyl)thiazol-2-amine synthesis

2synthesis methods
-

Yield:136343-79-8 95%

Reaction Conditions:

with toluene-4-sulfonic acid in isopropyl alcohol at 80; for 48 h;

Steps:

General procedure for nucleophilic substitution reactions towards compounds 3 - 12

General procedure: 1.0 equiv of the halothiazole, 1.5 equiv of the amino-substrate and 0.5 equiv of p-toluenesulfonic acid were dissolved in i-propanol and the reaction mixture was stirred at 80 °C until the reaction was complete (TLC). The reaction mixture was then diluted with ethyl acetate and washed with saturated NaHCO3 solution and brine followed by general work-up. Purification was carried out by Kugelrohr distillation.

References:

Schnürch, Michael;Waldner, Birgit;Hilber, Karlheinz;Mihovilovic, Marko D. [Bioorganic and Medicinal Chemistry Letters,2011,vol. 21,# 7,p. 2149 - 2154] Location in patent:experimental part