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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069045Generated: October 30, 2026

4-(1-(4-Nitronaphthalen-1-yloxy)ethyl)pyridin-2-amine → 4-(1-(4-Aminonaphthalen-1-yloxy)ethyl)pyridin-2-amine

https://huagongshe.com/reaction/2069045

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(1-(4-Nitronaphthalen-1-yloxy)ethyl)pyridin-2-amineHCID 58416782—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinumHCID 23939—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
Product4-(1-(4-Aminonaphthalen-1-yloxy)ethyl)pyridin-2-amineHCID 5841678099%

Reaction Steps

A solution of 4-(1-(4-Nitronaphthalen-1-yloxy)ethyl)pyridin-2-amine (38) (91 mg, 0.294 mmol) in MeOH (15 mL) and AcOH (3.0 mL) was passed through a Thales H-cube (1.0 mL·min−1, 30° C., 55 mm, 10% Pt/C Cat-Cart, full hydrogen mode). The volatiles were removed under reduced pressure, leaving a purple solid, which was then subjected to SCX capture and release to give the title compound (39) (81 mg, 99%) as a purple oil: m/z 280 (M+H)+ (ES+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299073B2
Source datasetuspto-grants-2012_10
ORD IDord-77172f14cb7c48c4aa1bb3531912565a
Source noteuspto-grants-2012_10