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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296647Generated: October 31, 2026

HCID 11128927, compound → HCID 10967168, compound

https://huagongshe.com/reaction/2296647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11128927HCID 11128927—
CatalystAdams' catalystHCID 345198—
SolventAcetic AcidHCID 176—
SolventHCID 178418361HCID 178418361—
ProductHCID 10967168HCID 1096716890.3%

Reaction Steps

A solution of ethyl 1-tert-butoxycarbonyl-1,4,5,6-tetrahydropyrazine-2-carboxylate (69.0 g) in acetic acid (AcOH, 500 ml) was subjected to catalytic reduction using platinum dioxide (4.0 g) at 40° C. in hydrogen at 3 atm for 4 hours. The catalyst was removed by filtration, and the filtrate was concentrated in vacuo. The residue was dissolved in H2O (800 ml) and the solution was washed with Et2O (500 ml×2). To the aqueous layer was added NaHCO3 to adjust the pH of the solution to 8 and the solution was extracted with AcOEt (800 ml×2). The combined organic layer was washed with saturated aqueous NaHCO3 solution and brine, dried over MgSO4 and concentrated in vacuo to give 62.8 g of ethyl 1-tert-butoxycarbonyl-piperazine-2-carboxylate as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06489324B2
Source datasetuspto-grants-2002_12
ORD IDord-f9a66b797f4141678f82083925d26adc
Source noteuspto-grants-2002_12