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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872501Generated: October 30, 2026

3-(2-Pyridinyl)-1H-pyrazole-5-carboxylic acid → N-(2-(3-(4-cyano-3-nitrophenyl)-1H-pyrazol-1-yl)ethyl)-3-(pyridin-2-yl)-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/872501

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(2-Pyridinyl)-1H-pyrazole-5-carboxylic acidHCID 665156—
Reactant4-(1-(2-aminoethyl)-1H-pyrazol-3-yl)-2-nitrobenzonitrileHCID 67172577—
ProductN-(2-(3-(4-cyano-3-nitrophenyl)-1H-pyrazol-1-yl)ethyl)-3-(pyridin-2-yl)-1H-pyrazole-5-carboxamideHCID 70656199—

Reaction Steps

The title compound was prepared from 4-(1-(2-aminoethyl)-1H-pyrazol-3-yl)-2-nitrobenzonitrile (300 mg) and 3-(pyridine-2-yl)-1H-pyrazole-5-carboxylic acid (161 mg) using the method of Example 34(d). Yield 166 mg. 1H-NMR (400 MHz; d6-DMSO): δ 3.75 (q, 2H), 4.43 (t, 2H), 7.09 (d, 1H), 7.31 (br. s, 1H), 7.39 (m, HA), 7.88-7.96 (m, 3H), 8.20 (d, 1H), 8.37 (dd, 1H), 8.47-8.57 (m, 1H), 8.64 (m, 1H), 8.71 (d, 1H), 13.90 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975254B2
Source datasetuspto-grants-2015_03
ORD IDord-4519f88f10e84de0a02bfe9cb19702ab
Source noteuspto-grants-2015_03