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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850392Generated: November 1, 2026

tert-Butyl 5-cyano-6-methylpyridin-2-ylcarbamate → tert-Butyl 5-(aminomethyl)-6-methylpyridin-2-ylcarbamate

https://huagongshe.com/reaction/850392

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 5-cyano-6-methylpyridin-2-ylcarbamateHCID 10704790—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
Producttert-Butyl 5-(aminomethyl)-6-methylpyridin-2-ylcarbamateHCID 10681361—

Reaction Steps

A mixture of 2-t-butoxycarbonylamino-5-cyano-6-methylpyridine (14.68 g, 62.9 mmol) and 10% Pd/C (1.5 g) in glacial acetic acid (150 ml) was shaken on a Parr apparatus at 60 psi for 88 h. The reaction was filtered through celite and was evaporated in vacuo. The residue was dissolved in water and the solution was washed with methylene chloride (2 times), then was basified with sodium carbonate and extracted with ethyl acetate (2 times). The combined ethyl acetate layers were dried (Na2SO4) and evaporated in vacuo to a solid. The crude product was recrystallized (ethyl acetate/hexanes) to give the title compound:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06017934
Source datasetuspto-grants-2000_01
ORD IDord-49e0fd16faea4c1fab9abd42f2ac56f8
Source noteuspto-grants-2000_01