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2-nitro-5-(pyrrolidin-1-yl)pyridine synthesis

1synthesis methods
39856-50-3 Synthesis
5-Bromo-2-nitropyridine

39856-50-3
525 suppliers
$6.00/5g

2-nitro-5-(pyrrolidin-1-yl)pyridine

1448988-13-3
12 suppliers
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Yield:1448988-13-3 410 mg

Reaction Conditions:

at 120; for 1 h;Microwave irradiation;

Steps:

25.1 Step 25.1 : 2-Nitro-5-pyrrolidin-1 -ylpyridine

Step 25.1 : 2-Nitro-5-pyrrolidin-1 -ylpyridine A mixture of 600 mg (2.93 mmol) of 5-bromo-2-nitropyridine and 1 .05 g (14.63 mmol) of pyrrolidine is heated in a Biotage microwave machine for 1 hour at 120°C. The reaction medium is diluted with water and then extracted with ethyl acetate. The organic phase is washed twice with water, dried over MgS04 and then filtered. The filtrate is evaporated under reduced pressure and then chromatographed on silica gel, eluting with a heptane/ethyl acetate mixture from (100/0 v/v) up to (50/50 v/v) to give 410 mg of 2- nitro-5-pyrrolidin-1-ylpyridine.

References:

WO2013/111106,2013,A1 Location in patent:Page/Page column 113