Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874363Generated: October 25, 2026

Tert-butyl 3-(6-nitropyridin-3-yloxy)phenylcarbamate → Tert-butyl 3-(6-aminopyridin-3-yloxy)phenylcarbamate

https://huagongshe.com/reaction/1874363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 3-(6-nitropyridin-3-yloxy)phenylcarbamateHCID 57749209—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductTert-butyl 3-(6-aminopyridin-3-yloxy)phenylcarbamateHCID 57749334106.6%

Reaction Steps

In the same manner as in Reference Example 34 and using tert-butyl {3-[(6-nitropyridin-3-yl)oxy]phenyl}carbamate (16.4 g, 49.5 mmol), palladium carbon (50% water-containing product, 1.50 g) and methanol (100 mL) as starting materials, the title compound (15.9 g, quant.) was obtained as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304557B2
Source datasetuspto-grants-2012_11
ORD IDord-a02cc20b73f54b1aa2c9721bf3bc5b73
Source noteuspto-grants-2012_11