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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1916713Erstellt: 26. Oktober 2026

Cyclopropanemethanamine, N-propyl- → (2-{5-[5-(4-Chloro-phenyl)-pyridin-2-ylethynyl]-indol-1-yl}-ethyl)-cyclopropylmethyl-propyl-amine

https://huagongshe.com/reaction/1916713

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyclopropanemethanamine, N-propyl-HCID 117787—
Edukt2-{5-[5-(4-Chloro-phenyl)-pyridin-2-ylethynyl]-indol-1-yl}-ethyl methanesulphonateHCID 86594684—
LösungsmittelDimethylformamideHCID 6228—
Produkt(2-{5-[5-(4-Chloro-phenyl)-pyridin-2-ylethynyl]-indol-1-yl}-ethyl)-cyclopropylmethyl-propyl-amineHCID 59835856—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

63 μL (0.44 mmol) cyclopropylmethyl-propyl-amine are added to a solution of 100 mg (0.22 mmol) 2-{5-[5-(4-chloro-phenyl)-pyridin-2-ylethynyl]-indol-1-yl}-ethyl methanesulphonate in 2 mL DMF and the reaction mixture is stirred for 16 h at 60° C. The mixture is evaporated down i. vac., the residue is taken up in DCM, the organic phase is washed with water and dilute K2CO3 solution and dried over Na2SO4. After the desiccant and solvent have been eliminated the residue is purified twice by chromatography (Alox, cyc/EtOAc 8:2 and cyc/DCM 1:1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08618132B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-2d02db9d770249e3a9cffc7753d750c6
Quellennotizuspto-grants-2013_12