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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502170Generated: October 30, 2026

tert-Butyl (5-nitropyridin-2-yl)carbamate → tert-butyl N-(5-aminopyridin-2-yl)carbamate

https://huagongshe.com/reaction/1502170

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl (5-nitropyridin-2-yl)carbamateHCID 11064480—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
Producttert-butyl N-(5-aminopyridin-2-yl)carbamateHCID 22064440—

Reaction Steps

tert-Butyl 5-nitropyridin-2-ylcarbamate (750 mg, 3.14 mmol) was suspended in AcOH at RT with vigorously stirring. Zinc (2051 mg, 31.4 mmol) was added slowly (exothermic reaction). The mixture was stirred at RT for 20 min, and filtered. The filter cake was washed with ethyl acetate. The filtrate was concentrated to give tert-butyl 5-aminopyridin-2-ylcarbamate: LC/MS: [(M+1-56)]+=154.16.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206199B2
Source datasetuspto-grants-2015_12
ORD IDord-3008d110058c4464b0f79ede1b00bf10
Source noteuspto-grants-2015_12