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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 242195Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/242195

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktHydrazineHCID 9321—
Edukt(4-Methoxyphenyl)hydrazineHCID 77023—
Edukt(1-Ethoxyethylidene)malononitrileHCID 79450—
LösungsmittelEthanolHCID 702—
Produkt5-amino-1-(4-methoxyphenyl)-3-methyl-1H-pyrazole-4-carbonitrileHCID 6712004190,8%

Reaktionsbedingungen

Temperatur105 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08653112B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-60cd323482e643bdbe1183d98b1166c6
Quellennotizuspto-grants-2014_02