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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1472874Erstellt: 24. Oktober 2026

N-(2-(p-bromophenoxy)ethyl)pyrrolidine → HCID 59589976, Verbindung

https://huagongshe.com/de/reaction/1472874

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-(2-(p-bromophenoxy)ethyl)pyrrolidineHCID 70657—
Edukt1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
EduktSodium t-butoxideHCID 23676156—
Edukt5-(2,3-Dihydro-benzo[1,4]dioxin-6-yl)-6-methoxy-[1,2,4]triazolo[1,5-a]pyridin-2-ylamineHCID 59589684—
KatalysatorDimethylacetamideHCID 31374—
Katalysator(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktHCID 59589976HCID 59589976—

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

In a microwave vial, 5-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-6-methoxy-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine (0.05 g, 0.17 mmol), 1-[2-(4-bromophenoxy)ethyl]-pyrrolidine (0.068 g, 0.251 mmol), bis(dibenzylideneacetone)palladium (0.005 g, 0.008 mmol), Xantphos (0.01 g, 0.017 mmol) and sodium tert-butoxide (0.033 g, 0.335 mmol) were added successively. Dioxane (1.2 mL) and dimethylacetamide (2 drops) were added and the vial was sealed and heated in the microwave (150° C., 10 min). The crude was purified using an SCX cartridge, by washing with methanol and releasing the compound with 2M ammonia in methanol. After concentration under reduced pressure, the crude was purified by preparatory LCMS. LCMS Method: 2: RT: 2.52 min, MI: 488 [M+1].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09012633B2
Quelldatensatzuspto-grants-2015_04
ORD IDord-5c5e2e70bf91492fbd9b29cdbe57ac50
Quellennotizuspto-grants-2015_04