Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898982Generated: October 29, 2026

3-Aminophenol → 4-(3-Aminophenoxy)pyridine-2-carboxamide

https://huagongshe.com/reaction/898982

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AminophenolHCID 11568—
Reactant4-Chloropyridine-2-carboxamideHCID 303543—
SolventDimethylacetamideHCID 31374—
Product4-(3-Aminophenoxy)pyridine-2-carboxamideHCID 23137229—

Reaction Steps

Entry 12: 4-Chloropyridine-2-carbonyl chloride HCl salt was reacted with ammonia according to Method A2, Step 3b to form 4-chloro-2-pyridinecarboxamide. 4-Chloro-2-pyridinecarboxamide was reacted with 3-aminophenol according to Method A2, Step 4 using DMAC in place of DMF to give 3-(2-carbamoyl-4-pyridyloxy)aniline. According to Method C2a, 2-methoxy-5-(trifluoromethyl)aniline was reacted with phosgene followed by 3-(2-carbamoyl-4-pyridyloxy)aniline to afford the urea.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07351834B1
Source datasetuspto-grants-2008_04
ORD IDord-70c1c890339f417da6d39b7420d933fb
Source noteuspto-grants-2008_04