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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494021Generated: October 24, 2026

Water → Tert-butyl 4-(6-nitropyridin-3-yl)piperazine-1-carboxylate

https://huagongshe.com/en/reaction/494021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant5-Bromo-2-nitropyridineHCID 817620—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-(6-nitropyridin-3-yl)piperazine-1-carboxylateHCID 1124375833%

Reaction Conditions

Temperature120 °C

Reaction Steps

A solution is prepared of 1 g (4.9 mM) of 2-nitro-5-bromopyridine and 917 mg (4.9 mM) of N-Boc-piperazine in 10 ml of dimethylformamide and 1.02 g (7.4 mM) of potassium carbonate are added. The reaction mixture is agitated at 120° C. for 36 hours and then cooled. 50 ml of water are then added and extraction is carried out with ethyl acetate. The organic phase obtained is washed with water, dried and concentrated under reduced pressure. The crude product is purified by silica gel chromatography in eluting with the aid of a toluene/isopropanol mixture (98/2; v/v). The product sought after is thus obtained as a yellow solid (yield=33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538111B2
Source datasetuspto-grants-2009_05
ORD IDord-be504eb9429b40eaa9d3ea8ff4b4dd3b
Source noteuspto-grants-2009_05