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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2298023Erstellt: 24. Oktober 2026

Guanidine Hydrochloride → HCID 178429413, Verbindung

https://huagongshe.com/de/reaction/2298023

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktGuanidine HydrochlorideHCID 5742—
EduktThionyl ChlorideHCID 24386—
Edukt1-(3-chlorophenyl)-5-methyl-1H-pyrazole-4-carboxylic acidHCID 4423672—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelSodium HydroxideHCID 14798—
ProduktHCID 178429413HCID 17842941312,7%

Reaktionsschritte

A mixture of 5-methyl-1-(3-chlorophenyl)pyrazole-4-carboxylic acid (234 mg, 1.0 mmol) and 5 ml SOCl2 was heated to reflux for 45 min. Excess SOCl2 was removed in vacuo via codistillation with toluene. The residue was dissolved in 2mL of anhydrous THF and added dropwise over 30 minutes to a vigorously stirred 40° C. solution of guanidine hydrochloride (344 mg, 3.6 mol) in 3.25 mL 2 N NaOH and 1.9 mL THF. The resulting mixture was heated to reflux for 4 hours and then cooled. The organic solvent was removed in vacuo. The residue was diluted with 10 mL 1 N NaOH and extracted with 5×5 mL EtOAc. The combined organic layers were dried (Na2SO4) filtered and concentrated in vacuo to a white solid. This material was dissolved in 1 mL MeOH and 18.4 μL 12 N HCl was added with stirring. The solvents were removed in vacuo with toluene azeotropes and the resulting solid was stirred in 1 mL ether/acetone (1:1) and filtered to remove residual H2O. Drying under high vacuum at 40° C. afforded the desired product (20 mg, 6%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06492401B1
Quelldatensatzuspto-grants-2002_12
ORD IDord-a3ff8d1a6c854a779f86a0b2b6980ea5
Quellennotizuspto-grants-2002_12