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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209272Generated: October 25, 2026

Diisopropylethylamine → 1,1-Dimethylethyl 4-(5-iodo-2-pyrazinyl)-1-piperazinecarboxylate

https://huagongshe.com/reaction/2209272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant2-Bromo-5-iodopyrazineHCID 21931200—
Solventtert-ButanolHCID 6386—
Product1,1-Dimethylethyl 4-(5-iodo-2-pyrazinyl)-1-piperazinecarboxylateHCID 86669229—

Reaction Conditions

Temperature100 °C

Reaction Steps

2-bromo-5-iodopyrazine (503 mg, 1.77 mmol) and tert-butyl piperazine-1-carboxylate (355 mg, 1.91 mmol) were taken up in tBuOH (8 mL). iPr2NEt (400 μL, 2.3 mmol) was added and the stirred reaction mixture was heated to 100° C. After 66 h, the reaction mixture was cooled and was partitioned between EtOAc, water and brine. The phases were separated, and the organic phase was dried over Na2SO4, filtered, and concentrated. The crude residue was purified by silica gel chromatography (10-30% EtOAc in hexanes) to afford tert-butyl 4-(5-iodopyrazin-2-yl)piperazine-1-carboxylate 7.11.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376441B2
Source datasetuspto-grants-2016_06
ORD IDord-a53a06b1ed774fd19e6d7b53c443e10b
Source noteuspto-grants-2016_06