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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407619Generated: October 30, 2026

Water → tert-butyl (3S)-3-methyl-4-(6-nitropyridin-3-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/407619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-2-nitropyridineHCID 817620—
Reactant(S)-1-Boc-3-methylpiperazineHCID 7023035—
SolventDimethyl SulfoxideHCID 679—
Producttert-butyl (3S)-3-methyl-4-(6-nitropyridin-3-yl)piperazine-1-carboxylateHCID 8668372850%

Reaction Conditions

Temperature65 °C

Reaction Steps

Into a solution of 5-bromo-2-nitropyridine (30 g, 148 mmol) in DMSO (350 mL) were added K2CO3 (14 g, 104 mmol) and (3S)-tert-butyl-3-methylpiperazine-1-carboxylate (10.0 g, 50 mmol). The mixture was stirred at 65° C. overnight and then after cooling to room temperature, poured into water (700 mL). The solid precipitate was collected and dried under vacuum. It was further purified on a flash column eluting with 20:1 petroleum ether/ethyl acetate and then with CH2Cl2 to give 105a as a yellow solid (8.05 g, 50%). LCMS: [M+H]+ 323

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754077B2
Source datasetuspto-grants-2014_06
ORD IDord-9156771e3abc40808517fa8ca3942087
Source noteuspto-grants-2014_06