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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744664Generated: October 26, 2026

1-(4-bromophenyl)-5-methyl-1H-pyrazole-4-carboxylic acid → 1-(4-Bromophenyl)-N-{3-cyano-4-[4-(3,4,5,6-tetrahydro-2H-pyran-4-yl)piperazin-1-yl]phenyl}-5-methylpyrazole-4-carboxamide

https://huagongshe.com/reaction/1744664

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-bromophenyl)-5-methyl-1H-pyrazole-4-carboxylic acidHCID 2769586—
Reactant5-amino-2-[4-(3,4,5,6-tetrahydro-2H-pyran-4-yl)piperazin-1-yl]benzonitrileHCID 21942323—
Product1-(4-Bromophenyl)-N-{3-cyano-4-[4-(3,4,5,6-tetrahydro-2H-pyran-4-yl)piperazin-1-yl]phenyl}-5-methylpyrazole-4-carboxamideHCID 2222801836.5%

Reaction Steps

By the reaction and treatment in the same manner as in Example 64 using 1-(4-bromophenyl)-5-methylpyrazole-4-carboxylic acid (1.0 g) and 5-amino-2-[4-(3,4,5,6-tetrahydro-2H-pyran-4-yl) piperazin-1-yl]benzonitrile (1.0 g), the title compound (0.7 g) was obtained, melting point: 288° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07015218B1
Source datasetuspto-grants-2006_03
ORD IDord-f2ef53501cea4c5282c93171c9309408
Source noteuspto-grants-2006_03