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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13447Generated: October 26, 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/13447

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 numberUS07728010B2
Source datasetuspto-grants-2010_06
ORD IDord-d53596ef137247da833ff0cac6ec958a
Source noteuspto-grants-2010_06