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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25170Erstellt: 25. Oktober 2026

Acetic Acid → HCID 22566248, Verbindung

https://huagongshe.com/reaction/25170

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt5-Amino-2-fluorobenzonitrileHCID 2737673—
Edukt1-[4-Bromophenyl]-3-hydroxy-4-acetyl-5,6-dihydropyridin-2-oneHCID 22566243—
EduktSodium NitriteHCID 23668193—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
ProduktHCID 22566248HCID 22566248—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

3-Cyano-4-fluoroaniline (3.7 mmol, 0.5 g) in conc. HCl (4 mL) was cooled to 0° C. and NaNO2 (4.4 mmol, 0.3 g) in water (3 mL). This was stirred at 0° C. for 30 min, then acetic acid (1.3 mL) was added. SnCl2·(H2O)2 (8.5 mmol, 1.9 g) in 1:1 water:conc. HCl (3 mL) was added dropwise to the cold solution and stirred for an additional 30 min. To this mixture 1-[4-bromophenyl]-3-hydroxy-4-acetyl-5,6-dihydropyridin-2-one (3.9 mmol, 1.2 g) was slurried in MeOH (20 mL) and added with the aid of additional MeOH (6 mL). The suspension was heated at 50° C. for 3 h, then cooled at 10° C. for 18 h. The product, 1-[3-cyano-4-fluorophenyl]-3-methyl-6-[4-bromophenyl]-1,4,5,6-tetrahydro-7H-pyrazolo[3,4-c]pyridin-7-one, was isolated by filtration. There was obtained 1.34 g (3.2 mmol) of product; mp 237.6° C., LRMS (M+H)+: 425.2/427.1 m/z.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06858616B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-12a5c411a99d44ab854390aad4e69c82
Quellennotizuspto-grants-2005_02