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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 38025Erstellt: 25. Oktober 2026

Dipropylamine → (1E,4E)-2-amino-8-bromo-N,N-dipropyl-3H-benzo[b]azepine-4-carboxamide

https://huagongshe.com/reaction/38025

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDipropylamineHCID 8902—
EduktPotassium Sodium TartrateHCID 9357—
EduktTrimethylaluminumHCID 16682925—
Eduktethyl 2-amino-8-bromo-3H-benzo[b]azepine-4-carboxylateHCID 58228535—
LösungsmittelTolueneHCID 1140—
Produkt(1E,4E)-2-amino-8-bromo-N,N-dipropyl-3H-benzo[b]azepine-4-carboxamideHCID 6696144634,1%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A 50 ml round bottom flask equipped with a stir bar and nitrogen inlet was charged with 15 mls of dry toluene and dipropylamine (0.44 ml, 3.24 mmol). This was chilled to 0° C. and AlMe3 (4.04 mls, 8.09 mmol, 2M in toluene) was then added. Once the addition was complete, the mixture was allowed to warm to room temperature (˜20-30 minutes). (1E,4E)-ethyl 2-amino-8-bromo-3H-benzo[b]azepine-4-carboxylate (0.5 g, 1.62 mmol) was then added portionwise resulting in a dark solution. This mixture was warmed to 100° C. for about 16 hours, and then allowed to cool to room temperature. This mixture was then poured into 50 mls of a 30% aq. solution of Rochelle's salt and vigorously stirred for 20 minutes, then extracted with EtOAc (2×), extracts dried over sodium sulfate and concentrated under reduced pressure. Flash 40 Biotage (40M cartridge, 5% MeOH/DCM) afforded 201 mgs (32%) of (1E,4E)-2-amino-8-bromo-N,N-dipropyl-3H-benzo[b]azepine-4-carboxamide. m/z (APCI-pos) M+1=364.2, 366.2.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524702B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-febcc2bbf55a49ebae7f0dc6f20e7b7e
Quellennotizuspto-grants-2013_09