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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634103Generated: October 31, 2026

1-(4-Aminophenyl)-3-(3-pyridyl)-5-cyanopyrazole → 6-[(3-Cyanopropoxy)]-N-[4-(5-cyano-3-pyridin-3-yl-pyrazol-1-yl)phenyl]nicotinamide

https://huagongshe.com/reaction/1634103

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Aminophenyl)-3-(3-pyridyl)-5-cyanopyrazoleHCID 18677106—
Reactant6-(3-Cyanopropyloxy)nicotinic acidHCID 18677116—
Product6-[(3-Cyanopropoxy)]-N-[4-(5-cyano-3-pyridin-3-yl-pyrazol-1-yl)phenyl]nicotinamideHCID 1867714063.2%

Reaction Steps

6-(3-cyanopropyloxy)nicotinic acid (0.6 mmol) was coupled with 3-(3-pyridyl)-5-cyano-1-(4′-aminophenyl)-pyrazole (0.5 mmol) under standard EDC mediated conditions (Method A). Standard work-up gave the title compound (142 mg, 62%), m.p. 190-191° C. 1H NMR(CDCl3): δ 2.04-2.11 (m, 2H), 2.67-2.70 (7, J=7.1 Hz, 2H), 4.42-4.5 (t, J=6.2 Hz, 2H), 6.98-7.00 (d, J=8.7 Hz, 1H), 7.53-7.56 (m, 1H), 7.82-7.84 (d, J=8.9 Hz, 2H), 8.02-8.04 (d, J=8.9 Hz, 2H), 8.1 (s, 1H), 8.28-8.32 (m, 2H), 8.63-8.64 (m, 1H), 8.82-8.83 (m, 1H), 9.15-9.16 (m, 1H), 10.6 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06506747B1
Source datasetuspto-grants-2003_01
ORD IDord-9367b35c435740ffa15725b5bc315a95
Source noteuspto-grants-2003_01