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66093-18-3

7-Bromo-1,5-naphthyridine-4-oxo-3-carboxylic acid ethyl ester synthesis

4synthesis methods
-

Yield:-

Reaction Conditions:

in diphenylether; for 1 h;Reflux;

Steps:

1.2 Ethyl 7-bromo-4-oxo-1,4-dihydro-1,5-naphthyridine-3-carboxylate

Step 2:
Ethyl 7-bromo-4-oxo-1,4-dihydro-1,5-naphthyridine-3-carboxylate
In a RBF fitted with a reflux condenser a mixture of diethyl 2-((5-bromopyridin-3-ylamino)methylene)malonate (1 g, 3 mmol) and 1-phenoxybenzene (10 mL, 63 mmol) was heated to reflux for 1 h.
The reaction mixture was allowed to cool to RT and CH3CN was added.
The resulting solids were filtered and dried to provide the desired product as a light brown solid.

References:

US2014/336182,2014,A1 Location in patent:Paragraph 0300

40131-09-7 Synthesis
diethyl methoxymethylenemalonate

40131-09-7
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7-Bromo-1,5-naphthyridine-4-oxo-3-carboxylic acid ethyl ester

66093-18-3
8 suppliers
inquiry