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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2218513Erstellt: 24. Oktober 2026

Diisopropylethylamine → 1-Acetyl-N-(3-(N-(4-(benzofuran-2-yl)thiazol-2-yl)thiophene-2-carboxamido)propyl)piperidine-4-carboxamide

https://huagongshe.com/de/reaction/2218513

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt1-Acetylpiperidine-4-carbonyl chlorideHCID 100950—
EduktN-(3-aminopropyl)-N-(4-(benzofuran-2-yl)thiazol-2-yl)thiophene-2-carboxamideHCID 68407996—
LösungsmittelChloroformHCID 6212—
Produkt1-Acetyl-N-(3-(N-(4-(benzofuran-2-yl)thiazol-2-yl)thiophene-2-carboxamido)propyl)piperidine-4-carboxamideHCID 68406261—

Reaktionsschritte

A mixture of the amine prepared above (77 mg, 0.2 mmol) and N,N-diisopropylethylamine (139 μL, 0.8 mmol) was dissolved in chloroform (2 mL), and a portion of the solution (200 μL, 0.02 mmol) was added to a solution of 1-acetyl-isonipecotoyl chloride (7.6 mg, 0.04 mmol) in chloroform (200 μL). The reaction mixture was maintained at room temperature overnight.). The reaction mixture was maintained at room temperature overnight, then concentrated in vacuo. The resulting residue was dissolved in DMSO (200 μL) and subjected to HPLC purification (Method Z) to provide the title compound (4.5 mg) as a yellowish solid. LC/MS (ESI) m/z 537.1 [M+H]. HPLC retention time (Method C)=3.44 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07410988B2
Quelldatensatzuspto-grants-2008_08
ORD IDord-4dfe5492e5094c07ae111d76eb72d2ae
Quellennotizuspto-grants-2008_08