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ETHYL 7-BROMO-[1,2,4]TRIAZOLO[1,5-A]PYRIDINE-2-CARBOXYLATE synthesis

2synthesis methods
Pyridinium, 1,2-diamino-4-bromo-, 2,4,6-trimethylbenzenesulfonate (1:1)

1202704-61-7
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4755-77-5 Synthesis
Ethyl chlorooxoacetate

4755-77-5
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$9.00/25g

ETHYL 7-BROMO-[1,2,4]TRIAZOLO[1,5-A]PYRIDINE-2-CARBOXYLATE

1380331-36-1
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Yield:1380331-36-1 60.5%

Reaction Conditions:

with pyridine at 100; for 18 h;

Steps:

33.a

a) ethyl 7-bromo-[1,2,4]triazolo[1,5-a]pyridine-2-carboxylate A mixture of 1,2-diamino-4-bromopyridinium2,4,6-trimethylbenzenesulfonate (4.18 g, 10.8 mmol) and ethyl 2-chloro-2-oxoacetate (2.4 ml, 21.5 mmol) in pyridine (25 ml) is heated for 18 hours to 100° C. The solvent is evaporated and the orange residue triturated with sat. aqueous sodium hydrogencarbonate solution for 2 hours. The solid is collected by filtration, washed several times with water and dried affording ethyl 7-bromo-[1,2,4]triazolo[1,5-a]pyridine-2-carboxylate (1.759 g, 60.5%) as a light pink solid. mp.: 158-160° C. MS: m/z=270.2 (M+H+).

References:

US2012/142665,2012,A1 Location in patent:Page/Page column 30