Solid phase synthesis of novel biaryl triazine library by...

Organic compounds -- part of the class 532-570 series – Organic compounds – Four or more ring nitrogens in the bicyclo ring system

Reexamination Certificate

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C544S206000, C544S213000

Reexamination Certificate

active

07115737

ABSTRACT:
Two methods are used to produce diaryl trisubstituted triazines. In the first method, cyanuric chloride is first reacted with a 4-alkoxybenzylamine. The product of this reaction is then reacted with a resin-bound amine, such as 4-alkoxybenzylamine, to ensure that the final compound will be bound to a resin. The product of this reaction is then reacted with boronic acid to produce a trisubstituted diaryl triazine. In the second method, cyanuric chloride is reacted with a benzenealkanethiol. The product of this reaction is then reacted with a resin-bound amine, such as 4-alkoxybenzylamine, to ensure that the final compound will be bound to a resin. The product of this reaction is then reacted with m-CPBA to form a sulfone, which is then reacted with a 4-alkoxybenzylamine to form the desired trisubstituted biaryltriazine.

REFERENCES:
patent: WO 03/032903 (2003-04-01), None
patent: WO 03/050237 (2003-06-01), None
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Schareina, T., et al., Combinatorial Libraries with P-functionalized aminopyridines: Ligands for the Preparation of Efficient C(aryl)-CI Activation Catalysts, Angewandte Chemi, Interantional Edition, 2002, pp. 1521-1523, vol. 41, No. 9.

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