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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271541Generated: November 1, 2026

Tert-butyl methyl(1-(5-nitropyridin-2-yl)piperidin-3-yl)carbamate → Tert-butyl (1-(5-aminopyridin-2-yl)piperidin-3-yl)(methyl)carbamate

https://huagongshe.com/reaction/2271541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl methyl(1-(5-nitropyridin-2-yl)piperidin-3-yl)carbamateHCID 71646997—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl (1-(5-aminopyridin-2-yl)piperidin-3-yl)(methyl)carbamateHCID 8669285196%

Reaction Steps

To a solution of tert-butyl methyl(1-(5-nitropyridin-2-yl)piperidin-3-yl)carbamate (1.03 g, 3.1 mmol) in THF (50 mL) was added Pd/C (10 wt. %, 500 mg). The reaction mixture was stirred under 1 atm of hydrogen for 16 h, filtered through celite and concentrated to afford the desired product (902 mg, 96%) as a red oil. ESI MS m/z 307 [C16H26N4O2+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120749B2
Source datasetuspto-grants-2015_09
ORD IDord-00a4af87799e4633b9cb8d9411b8f8a3
Source noteuspto-grants-2015_09