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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598469Generated: October 26, 2026

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

https://huagongshe.com/reaction/598469

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AminophenolHCID 11568—
Reactant4-Chloropyridine-2-carboxamideHCID 303543—
SolventDimethylformamideHCID 6228—
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 DISC 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 numberUS07897623B2
Source datasetuspto-grants-2011_03
ORD IDord-9c24e31243cb432f975a6a4e5cd48f8d
Source noteuspto-grants-2011_03