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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 524879Generated: October 30, 2026

HCID 86720935, compound → HCID 86720936, compound

https://huagongshe.com/reaction/524879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86720935HCID 86720935—
CatalystPalladiumHCID 23938—
CatalystZinc bromideHCID 10421208—
SolventMethanolHCID 887—
ProductHCID 86720936HCID 86720936—

Reaction Steps

To a solution of tert-butyl 4-(3-chloro-5-nitropyridin-4-yl)piperazine-1-carboxylate (900 mg, 2.626 mmol) and ZnBr2 (118.3 mg, 28.16 μL, 0.5252 mmol) in methanol (27.00 mL) was added Pd on C (10%, wet, Degussa) (300 mg). The reaction mixture was stirred at RT for 4 h under an atmosphere of hydrogen (balloon). The catalyst was filtered off and the filtrate was concentrated in vacuo to yield tert-butyl 4-(3-amino-5-chloropyridin-4-yl)piperazine-1-carboxylate which was used without further purification (820 mg, 99%). MS (ES+) 313.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340546B2
Source datasetuspto-grants-2016_05
ORD IDord-ca6820923466450082d6c89e90c6d781
Source noteuspto-grants-2016_05