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Ethyl 5-bromo-2-((2-methoxyethyl)amino)pyrimidine-4-carboxylate synthesis

3synthesis methods
74840-38-3 Synthesis
4-PyriMidinecarboxylic acid, 5-broMo-2-(Methylthio)-, ethyl ester

74840-38-3
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Ethyl 5-bromo-2-((2-methoxyethyl)amino)pyrimidine-4-carboxylate

1316122-39-0
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Yield:1316122-39-0 89%

Reaction Conditions:

in dichloromethane at 20 - 45; for 2 h;

Steps:

A.2

Step 2: 5-Bromo-2-(2-methoxy-ethylamino)-pyrimidine-4-carboxylic acid ethyl ester2-Methoxyethylamine (0.278 ml, 3.2 mmol) was added at room temperature to a solution of 5- bromo-2-methanesulfonyl-pyrimidine-4-carboxylic acid ethyl ester (0.2 g, 0.65 mmol) in dichloromethane (5 ml). Stirring was continued at 45 °C for 2 hours. The solvent was evaporated and the crude product was purified by silica gel chromatography using an ethyl acetate/heptane eluent to yield the title compound as colorless oil (0.175 g, 89 %).MS: M = 304.2 (M+H)+

References:

WO2011/89132,2011,A1 Location in patent:Page/Page column 55

1316122-36-7 Synthesis
Ethyl 5-bromo-2-(methylsulfonyl)pyrimidine-4-carboxylate

1316122-36-7
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Ethyl 5-bromo-2-((2-methoxyethyl)amino)pyrimidine-4-carboxylate

1316122-39-0
4 suppliers
inquiry