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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776998Generated: November 1, 2026

HCID 178460521, compound → HCID 178523894, compound

https://huagongshe.com/reaction/1776998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178460521HCID 178460521—
SolventEthanolHCID 702—
ProductHCID 178523894HCID 17852389483.2%

Reaction Conditions

Temperature40 °C

Reaction Steps

3-Chloro-N-(((3-chloro-5-fluorophenyl)amino)((5-(trifluoromethyl)-1H-pyrazol-3-yl)amino)methylene)benzamide acetone solvate (176 g) was dissolved in EtOH (875 mL) and warmed to 40° C. The mixture was clarified by filtration through celite and then diluted with EtOH/water (1/1 mixture by volume, 175 mL) at 40° C. Form II crystals of 3-chloro-N-(((3-chloro-5-fluorophenyl)amino)((5-(trifluoromethyl)-1H-pyrazol-3-yl)amino)methylene)benzamide (437 mg) were added to the mixture. Next, the suspension was further diluted with EtOH/water (1/1 mixture by volume, 700 mL) at 40° C. over 40 minutes, and then the mixture was allowed to cool to room temperature and stirring was continued overnight. Finally, the resulting suspension was filtered, the isolated residue was rinsed with EtOH/water (1/1 mixture by volume, 500 mL) and dried (60° C./10 Torr) to afford 130 g (74% recovery) of 3-chloro-N-(((3-chloro-5-fluorophenyl)amino)((5-(trifluoromethyl)-1H-pyrazol-3-yl)amino)methylene)benzamide as crystalline solid Form II. Analytical analysis did not identify solvate molecules in the crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266839B2
Source datasetuspto-grants-2016_02
ORD IDord-8d5c9bd769384c718ffe17c6b900ac45
Source noteuspto-grants-2016_02