Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42499Generated: October 28, 2026

Tert-butyl ((5-cyano-6-methoxy-4-methylpyridin-2-yl)methyl)carbamate → Tert-butyl ((5-(aminomethyl)-6-methoxy-4-methylpyridin-2-yl)methyl)carbamate

https://huagongshe.com/reaction/42499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl ((5-cyano-6-methoxy-4-methylpyridin-2-yl)methyl)carbamateHCID 86696542—
CatalystNickelHCID 935—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductTert-butyl ((5-(aminomethyl)-6-methoxy-4-methylpyridin-2-yl)methyl)carbamateHCID 6795165388%

Reaction Steps

A clear solution of tert-butyl((5-cyano-6-methoxy-4-methylpyridin-2-yl)methyl)carbamate (0.65 g, 2.344 mmol) in HOAc (5 mL) and Ethanol (20 mL) was treated on an H-Cube apparatus (50 psi, 40° C., 1 mL/min., Raney Nickel cartridge) for 18 hr overnight. LCMS showed that the reaction was complete. The reaction was evaporated to dryness under vacuum. Purified by silica gel chromatography (Analogix, SF25-60 g, 0 to 10% (5% NH4OH/MeOH) in CH2Cl2). The pure fractions were combined and evaporated to dryness under vacuum to give the product tert-butyl((5-(aminomethyl)-6-methoxy-4-methylpyridin-2-yl)methyl)carbamate (0.58 g, 2.061 mmol, 88% yield) as a clear thick oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536179B2
Source datasetuspto-grants-2013_09
ORD IDord-f6e68028a2e047869aa1f7c55ad51a00
Source noteuspto-grants-2013_09