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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744601Generated: October 26, 2026

1-(4-chlorophenyl)-5-methyl-1H-pyrazole-4-carboxylic acid → 1-(4-Chlorophenyl)-N-[3-cyano-4-[4-(4-morpholinyl)-1-piperidinyl]phenyl]-5-methyl-1H-pyrazole-4-carboxamide

https://huagongshe.com/reaction/1744601

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-chlorophenyl)-5-methyl-1H-pyrazole-4-carboxylic acidHCID 2777166—
Reactant5-Amino-2-(4-morpholinopiperidin-1-yl)benzonitrileHCID 21942389—
Product1-(4-Chlorophenyl)-N-[3-cyano-4-[4-(4-morpholinyl)-1-piperidinyl]phenyl]-5-methyl-1H-pyrazole-4-carboxamideHCID 2222793133.5%

Reaction Steps

By the reaction and treatment in the same manner as in Example 64 using 1-(4-chlorophenyl)-5-methylpyrazole-4-carboxylic acid (2 g) and 5-amino-2-(4-morpholinopiperidin-1-yl)benzonitrile (2.2 g), 1-(4-chlorophenyl)-N-[3-cyano-4-(4-morpholinopiperidin-1-yl)phenyl]-5-methylpyrazole-4-carboxamide (1.3 g) was obtained, melting point: 249–250° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07015218B1
Source datasetuspto-grants-2006_03
ORD IDord-6c35264614384116b38b3891e56925f1
Source noteuspto-grants-2006_03