Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 593299Erstellt: 23. Oktober 2026

Acetic Acid → 1-(4-(((3,5-Dimethyl-1-phenyl-1H-pyrazol-4-yl)methyl)amino)phenyl)butan-1-one

https://huagongshe.com/de/reaction/593299

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt1-Butanone, 1-(4-aminophenyl)-HCID 15527—
Edukt1H-Pyrazole-4-carboxaldehyde, 3,5-dimethyl-1-phenyl-HCID 89179—
LösungsmittelDimethylacetamideHCID 31374—
LösungsmittelDichloromethane methanolHCID 21226129—
Produkt1-(4-(((3,5-Dimethyl-1-phenyl-1H-pyrazol-4-yl)methyl)amino)phenyl)butan-1-oneHCID 68722715—

Reaktionsbedingungen

Temperatur55 °C

Reaktionsschritte

In a 20 ml vial, to a solution of solution of 1-(4-aminophenyl)butan-1-one (46 mg, 0.28 mmol) dissolved in DCM/MeOH (0.6 mL) was added a solution of 3,5-dimethyl-1-phenyl-1H-pyrazole-4-carbaldehyde (112 mg, 0.56 mmol) in DMA (1.8 mL). A solution of acetic acid (50 mg, 0.84 mmol) in DCM/MeOH (0.6 mL) was then added, followed by the addition of 361 mg of MP-CNBH3 resin (3 eq.; subst. 2.34 mmoles/g). The vial was capped and was then heated with shaking overnight at 55° C. The progress of the reaction was monitored by LC/MS. After completion of the reaction, the reaction mixture was concentrated to dryness. The resulting residue was dissolved in 1:1 DMSO/MeOH. Purification by reverse phase HPLC (TFA method) gave the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09242933B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-753f62ebc22d4739aff3da88b7d0bec7
Quellennotizuspto-grants-2016_01