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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874373Generated: October 25, 2026

Tert-butyl {2-chloro-5-[(6-nitropyridin-3-yl)oxy]phenyl}carbamate → Tert-butyl {5-[(6-aminopyridin-3-yl)oxy]-2-chlorophenyl}carbamate

https://huagongshe.com/reaction/1874373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl {2-chloro-5-[(6-nitropyridin-3-yl)oxy]phenyl}carbamateHCID 57749305—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductTert-butyl {5-[(6-aminopyridin-3-yl)oxy]-2-chlorophenyl}carbamateHCID 5774935659%

Reaction Steps

To a solution of tert-butyl {2-chloro-5-[(6-nitropyridin-3-yl)oxy]phenyl}carbamate (13.5 g, 36.9 mmol) in methanol (500 mL) was added palladium carbon (50% water-containing product, 2.96 g), and the mixture was stirred under a hydrogen atmosphere at room temperature for 17 hr. The reaction mixture was filtered through celite, and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography (silica gel, hexane/ethyl acetate=100/0→75/25) to give the title compound (7.29 g, 59%) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304557B2
Source datasetuspto-grants-2012_11
ORD IDord-2b3c2fcb0a664a5badbe9d02c0b9e86c
Source noteuspto-grants-2012_11