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ethyl 5-bromo-3-((ethoxycarbonyl)amino)benzofuran-2-carboxylate synthesis

3synthesis methods
330555-71-0 Synthesis
3-AMINO-5-BROMO-BENZOFURAN-2-CARBOXYLIC ACID ETHYL ESTER

330555-71-0
40 suppliers
$117.00/100mg

ethyl 5-bromo-3-((ethoxycarbonyl)amino)benzofuran-2-carboxylate

1251582-36-1
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Yield:1251582-36-1 100%

Reaction Conditions:

in toluene;acetonitrile;Reflux;

Steps:

38.1

A mixture of the benzofuran 38a (prepared using the method of Example 1, step 1 but replacing compound 1a with 4-bromo-2-cyanophenol, and replacing compound 1b with ethyl 2-bromoacetate (6.0 g, 1 eq) in toluene/acetonitrile (75 mL/45 mL) and ethyl chloroformate (10 mL, 5 eq) is heated at reflux overnight, then concentrated under reduced pressure to give compound 38b (7.4 g, 100%).

References:

US2010/261714,2010,A1 Location in patent:Page/Page column 64