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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070249Generated: October 30, 2026

Tert-butyl 4-[4-(methylamino)-3-nitrophenoxy]pyridine-2-carboxylate → Tert-butyl4-[3-amino-4-(methylamino)phenoxy]pyridine-2-carboxylate

https://huagongshe.com/reaction/2070249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-[4-(methylamino)-3-nitrophenoxy]pyridine-2-carboxylateHCID 22040453—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductTert-butyl4-[3-amino-4-(methylamino)phenoxy]pyridine-2-carboxylateHCID 22040526—

Reaction Steps

A solution of tert-butyl 4-[4-(methylamino)-3-nitrophenoxy]pyridine-2-carboxylate (1 eq) and 10% palladium on carbon (0.1 eq) in methanol was stirred at room temperature and flushed with nitrogen. Hydrogen was flushed through the reaction for 1-2 hours or until the reaction was determined to be complete by HPLC. Nitrogen was flushed through the reaction for 15 minutes before the reaction was filtered through a celite pad. The celite pad was washed with excess methanol followed by concentration under reduced pressure to afford the product as a light yellow solid. MS: MH+=316.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299108B2
Source datasetuspto-grants-2012_10
ORD IDord-afc41c4e7ca84cce80e1d35c916bca73
Source noteuspto-grants-2012_10