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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266325Generated: October 26, 2026

2-(2-Methyl-6-(trifluoromethyl)pyridin-3-yl)acetic acid → N'-(5-(2-chlorophenyl)-4-(4-chlorophenyl)pyridin-2-yl)-2-(2-methyl-6-(trifluoromethyl)pyridin-3-yl)acetohydrazide

https://huagongshe.com/reaction/2266325

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-Methyl-6-(trifluoromethyl)pyridin-3-yl)acetic acidHCID 11557596—
Reactant5-(2-Chlorophenyl)-4-(4-chlorophenyl)-2-hydrazinylpyridineHCID 57799387—
ReactantN'-(6-(2-chlorophenyl)-5-(4-chlorophenyl)pyridazin-3-yl)-2-(4-(trifluoromethyl)phenyl)acetohydrazideHCID 57979748—
ProductN'-(5-(2-chlorophenyl)-4-(4-chlorophenyl)pyridin-2-yl)-2-(2-methyl-6-(trifluoromethyl)pyridin-3-yl)acetohydrazideHCID 57979742100.4%

Reaction Steps

The title compound (80 mg, 99%) as a white solid was prepared from 5-(2-chlorophenyl)-4-(4-chlorophenyl)-2-hydrazinylpyridine (50 mg, 0.15 mmol) and 2-(2-methyl-6-(trifluoromethyl)pyridin-3-yl)acetic acid (49.3 mg, 0.225 mmol) in a manner analogous to that in which N′-(6-(2-chlorophenyl)-5-(4-chlorophenyl)pyridazin-3-yl)-2-(4-(trifluoromethyl)phenyl)acetohydrazide (Example 11A) was prepared. HPLC/MS: retention time=3.63 min, [M+H]+=531.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858639B2
Source datasetuspto-grants-2010_12
ORD IDord-a5a4c92b57524028b45720dd7b1b3f9f
Source noteuspto-grants-2010_12