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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744641Generated: October 27, 2026

1-(4-chlorophenyl)-5-methyl-1H-pyrazole-4-carboxylic acid → N-[4-(1-Benzylpiperidin-4-yloxy)-3-cyanophenyl]-1-(4-chlorophenyl)-5-methylpyrazole-4-carboxamide

https://huagongshe.com/reaction/1744641

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-chlorophenyl)-5-methyl-1H-pyrazole-4-carboxylic acidHCID 2777166—
Reactant5-Amino-2-(1-benzylpiperidin-4-yloxy)benzonitrileHCID 21942352—
ProductN-[4-(1-Benzylpiperidin-4-yloxy)-3-cyanophenyl]-1-(4-chlorophenyl)-5-methylpyrazole-4-carboxamideHCID 2222812329.2%

Reaction Steps

By the reaction and treatment in the same manner as in Example 64 using 1-(4-chlorophenyl)-5-methylpyrazole-4-carboxylic acid (1.0 g) and 5-amino-2-(1-benzylpiperidin-4-yloxy)benzonitrile (1.2 g), the title compound (0.6 g) was obtained, melting point: 194° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07015218B1
Source datasetuspto-grants-2006_03
ORD IDord-0c5d5d48408c4c64b41b86bebd42031f
Source noteuspto-grants-2006_03