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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1483143Generated: October 25, 2026

Cesium carbonate → 4-(6-Nitropyridin-3-yl)-3-oxopiperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1483143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant5-Bromo-2-nitropyridineHCID 817620—
ReactantTert-butyl 3-oxopiperazine-1-carboxylateHCID 3157178—
Catalystpalladium(II) acetateHCID 167845—
Catalyst1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
Solvent1,4-DioxaneHCID 31275—
Product4-(6-Nitropyridin-3-yl)-3-oxopiperazine-1-carboxylic acid tert-butyl esterHCID 5929095277%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 5-bromo-2-nitropyridine (200 mg, 1 mmol), 1-Boc-3-oxopiperazine (240 mg, 1.2 mmol), Xantphos (43 mg, 0.075 mmol), cesium carbonate (326 mg, 1 mmol), palladium(II) acetate (11 mg, 0.049 mmol) in dioxane (5.5 mL) is heated to 120° C. in a Personal Chemistry microwave apparatus for 0.5 h. TLC and LCMS analysis indicates completion of the reaction. The reaction mixture is filtered through Celite, evaporated in vacuo, and the residue is partitioned between water and ethyl acetate. The organic layer is washed with brine, dried (Na2SO4) and evaporated in vacuo. Purification by flash chromatography on silica (ethyl acetate) provides 4-(6-Nitropyridin-3-yl)-3-oxopiperazine-1-carboxylic acid tert-butyl ester as a pale brown solid (248 mg, 77%). MS (ESI) m/z 323 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09416136B2
Source datasetuspto-grants-2016_08
ORD IDord-e9b8fc08827847c38b4bfdd8e2a4de51
Source noteuspto-grants-2016_08