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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361372Generated: October 30, 2026

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

https://huagongshe.com/reaction/361372

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 numberUS05866573
Source datasetuspto-grants-1999_02
ORD IDord-011006007f4e4d169fe762ec52a49e09
Source noteuspto-grants-1999_02