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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242195Generated: October 25, 2026

Hydrochloric Acid → 5-amino-1-(4-methoxyphenyl)-3-methyl-1H-pyrazole-4-carbonitrile

https://huagongshe.com/reaction/242195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydrazineHCID 9321—
Reactant(4-Methoxyphenyl)hydrazineHCID 77023—
Reactant(1-Ethoxyethylidene)malononitrileHCID 79450—
SolventEthanolHCID 702—
Product5-amino-1-(4-methoxyphenyl)-3-methyl-1H-pyrazole-4-carbonitrileHCID 6712004190.8%

Reaction Conditions

Temperature105 °C

Reaction Steps

To a stirred solution of 2-(1-ethoxyethylidene)malononitrile (1.00 g, 6.66 mmol) in EtOH (8 mL) was added (4-methoxyphenyl)hydrazine (1.29 g, 9.32 mmol). (Prior to use the hydrazine its HCl salt was washed with NaHCO3/CH2Cl2. The organic phase was concentrated and used directly.) The solution was heated to 105° C. in the microwave for 20 min. CH2Cl2 was added and the organic phase was washed with 1M HCl and the organic extract was washed with aqueous NaHCO3. The solution was dried using a phase separator and concentrated under reduced pressure to give 5-amino-1-(4-methoxyphenyl)-3-methyl-1H-pyrazole-4-carbonitrile (1.38 g, 85%) which was used as such in the next step. The procedure was adapted from J. Med. Chem. 2004, 47, 5894-5911.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653112B2
Source datasetuspto-grants-2014_02
ORD IDord-60cd323482e643bdbe1183d98b1166c6
Source noteuspto-grants-2014_02