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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598472Generated: October 26, 2026

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

https://huagongshe.com/reaction/598472

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminophenolHCID 403—
Reactant4-Chloropyridine-2-carboxamideHCID 303543—
SolventDimethylacetamideHCID 31374—
Product4-(4-Aminophenoxy)pyridine-2-carboxamideHCID 23088338—

Reaction Steps

Entry 14: 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 4-aminophenol according to Method A2, Step 4 using DMAC in place of DMF to give 4-(2-carbamoyl-4-pyridyloxy)aniline. According to Method C4,2-methoxy-5-(trifluoromethyl)aniline was reacted with phosgene followed by 4-(2-carbamoyl-4-pyridyloxy)aniline to afford the urea.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897623B2
Source datasetuspto-grants-2011_03
ORD IDord-773ce1bd9e5f458e804aed7614fa7d6a
Source noteuspto-grants-2011_03