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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645136Generated: October 26, 2026

4-Amino-2-chlorophenol → 4-(2-(N-methylcarbamoyl)4-pyridyloxy)-3-chloroaniline

https://huagongshe.com/reaction/1645136

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-2-chlorophenolHCID 77578—
Reactant4-Chloro-N-methylpicolinamideHCID 1476814—
Product4-(2-(N-methylcarbamoyl)4-pyridyloxy)-3-chloroanilineHCID 23614562—

Reaction Steps

Entry 97: According to Method A2, Step 4, 4-amino-2-chlorophenol was reacted with 4-chloro-N-methyl-2-pyridinecarboxamide, which had been synthesized according to Method A2, Step 3b, to give 4-(2-(N-methylcarbamoyl)-4-pyridyloxy)-3-chloroaniline. 4-Chloro-2-methoxy-5-(trifluoromethyl)aniline was synthesized according to Method A7. 4-Chloro-2-methoxy-5-(trifluoromethyl)aniline was converted into 4-chloro-2-methoxy-5-(trifluoromethyl)phenyl isocyanate according to Method B1. According to Method C1a, 4-chloro-2-methoxy-5-(trifluoromethyl)phenyl isocyanate was reacted with 4-(2-(N-methylcarbamoyl)-4-pyridyloxy)-3-chloroaniline to afford the urea.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124630B2
Source datasetuspto-grants-2012_02
ORD IDord-b1494e25e3884afa8fbf240943556174
Source noteuspto-grants-2012_02