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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634101Generated: October 31, 2026

4-(Cyanopropyloxy)benzoic acid → 4-(3-cyanopropoxy)-N-[4-(5-cyano-3-pyridin-3-yl-pyrazol-1-yl)phenyl]benzamide

https://huagongshe.com/reaction/1634101

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Cyanopropyloxy)benzoic acidHCID 14650336—
Reactant1-(4-Aminophenyl)-3-(3-pyridyl)-5-cyanopyrazoleHCID 18677106—
Product4-(3-cyanopropoxy)-N-[4-(5-cyano-3-pyridin-3-yl-pyrazol-1-yl)phenyl]benzamideHCID 9803703—

Reaction Steps

The 4-(cyanopropyloxy)benzoic acid (0.75 mmol) was coupled with 3-(3-pyridyl)-5-cyano-1-(4′-aminophenyl)-pyrazole (0.5 mmol) under standard EDC mediated conditions (Method A). The crude product was recrystallized from hot benzene/methanol, m.p. 193-194° C. 1H NMR(CDCl3): δ 2.04-2.11 (m, 2H), 2.68-2.71 (7, J=7.1 Hz, 2H), 4.14-4.17 (t, J=6 Hz, 2H), 7.11-7.13 (d, J=8.6 Hz, 2H), 7.53-7.56 (m, 1H), 7.79-7.82(d, J=8.7 Hz, 2H), 8.00-8.05 (m, 4H), 8.1 (s, 1H), 8.30-8.32 (d, J=8 Hz, 1H), 8.63-8.64(d, J=4.6 Hz, 1H), 9.15 (s, 1H), 10.4 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06506747B1
Source datasetuspto-grants-2003_01
ORD IDord-bdfa8440a492474e9ec2851b3b41de09
Source noteuspto-grants-2003_01