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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 883047Erstellt: 25. Oktober 2026

Benzyl Bromide → 1-benzyl-1H-pyrazol-3-amine

https://huagongshe.com/reaction/883047

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl BromideHCID 7498—
EduktSodium hydrideHCID 24758—
EduktHCID 178514958HCID 178514958—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-benzyl-1H-pyrazol-3-amineHCID 150861632%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

3.1 2-(1H-Pyrazole-3-yl)-isoindole-1,3-dione (11.7 mmol) is added to a suspension of NaH (2 eq.) in DMF at 0° C. Benzylbromide (1 eq.) is added and the reaction is stirred 15 h at 50° C. The solvent is removed in vacuo. Hydrazine hydroxide (10 ml) and ethanol (20 ml) are added and the reaction is stirred 17 hours at 120° C. The precipitate is filtered and the solvent is removed in vacuo. The residue is suspended in dichloromethane and filtrated. The solvent of the filtrate is removed in vacuo. The remaining residue is purified via column chromatography (Ethyl acetate/methanol). 1-Benzyl-1H-pyrazole-3-ylamine is isolated as a yellow powder in a yield of 32%; HPLC (Method B): 2.45 min; LC-MS (Method B): 1.203 min, 174.15 (M+H+);

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08236824B2
Quelldatensatzuspto-grants-2012_08
ORD IDord-d65f0c7dc5fa45feb0aaf321b69d9ab7
Quellennotizuspto-grants-2012_08