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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2080328Erstellt: 25. Oktober 2026

Diisopropylethylamine → 2-[4-(dimethylamino)phenyl]-N-{[3'-(1-piperazinylmethyl)-3-biphenylyl]methyl}acetamide

https://huagongshe.com/reaction/2080328

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt4-N,N-dimethylaminophenylacetic acidHCID 152203—
EduktPyBOPHCID 2724699—
EduktHCID 67101934HCID 67101934—
LösungsmittelChloroform trifluoroacetic acidHCID 19978452—
Produkt2-[4-(dimethylamino)phenyl]-N-{[3'-(1-piperazinylmethyl)-3-biphenylyl]methyl}acetamideHCID 5773670147,1%

Reaktionsschritte

A mixture of PyBOP (0.08 mmol in 200 mL of DMF), {[3′-(1-piperazinylmethyl)-3-biphenylyl]methyl}amine (44 mmol in 200 mL of DMF) and DIPEA (30 mL) were added to [4-(dimethylamino)phenyl]acetic acid (0.07 mmol). The resulting mixture was stirred for 16 hours at room temperature, then the solvent was removed under vacuum. The residue was dissolved in methanol and purified by loading onto a SPE cartridge (SCX, 500 mg), washing with MeOH, and eluting with a 2 M solution of NH3 in MeOH. The NH3 fraction was collected and evaporated under vacuum to give a gum which was dissolved in 1:1 CHCl3/TFA (0.5 mL). After stirring for 2 hours, the solvent was removed under vacuum and the residue was dissolved in MeOH. The free base of the compound was obtained by loading the solution onto a SPE cartridge (SCX, 500 mg), washing with MeOH, and eluting with 2M NH3/MeOH. The ammonia fraction was collected and the solvent was removed under vacuum to give the title compound (14.6 mg). LC/MS: m/z, 443 (M+H), 2.21 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07932247B2
Quelldatensatzuspto-grants-2011_04
ORD IDord-439de902695e460cb1ff45af2cd76549
Quellennotizuspto-grants-2011_04