Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696485Generated: October 31, 2026

Pentanenitrile, 4,4-dimethyl-3-oxo- → ethyl 3-(5-amino-3-t-butyl-1H-pyrazol-1-yl)-1-naphthoate

https://huagongshe.com/reaction/1696485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentanenitrile, 4,4-dimethyl-3-oxo-HCID 108871—
ReactantEthyl 3-hydrazinonaphthalene-1-carboxylate hydrochlorideHCID 67271149—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
Productethyl 3-(5-amino-3-t-butyl-1H-pyrazol-1-yl)-1-naphthoateHCID 5885168295.3%

Reaction Steps

A mixture of 3-hydrazinonaphthalene-1-carboxylic acid ethyl ester hydrochloride (1.5 g, 5.6 mmol) and 4,4-dimethyl-3-oxopentanenitrile (875 mg, 7.0 mmol) in EtOH (50 mL) and conc. HCl (5 mL) was heated at reflux overnight. After removal of the solvent, the residue was purified by column chromatography to yield ethyl 3-(5-amino-3-t-butyl-1H-pyrazol-1-yl)-1-naphthoate (1.8 g, 95% yield). 1H NMR (300 MHz, DMSO-d6): δ 8.74 (d, J=6.3 Hz, 1H), 8.47 (s, 1H), 8.24 (s, 1H), 8.15 (d, J=6.0 Hz, 1H), 7.76 (t, J=5.7 Hz, 1H), 7.71 (t, J=5.7 Hz, 1H), 5.68 (s, 1H), 4.44 (q, J=5.4 Hz, 2H), 1.37 (t, J=5.4 Hz, 3H), 1.30 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163756B2
Source datasetuspto-grants-2012_04
ORD IDord-cb1abdcf015d40cf81e2b326efb74600
Source noteuspto-grants-2012_04