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HRID 241208Erstellt: 25. Oktober 2026

Diisopropylethylamine → 4-[6,7-Bis(methyloxy)quinolin-4-yl]-7-bromo-2,3,4,5-tetrahydro-1,4-benzoxazepine

https://huagongshe.com/reaction/241208

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt4-Chloro-6,7-dimethoxyquinolineHCID 459610—
Edukt7-Bromo-2,3,4,5-tetrahydro-1,4-benzoxazepine hydrochlorideHCID 66820137—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt4-[6,7-Bis(methyloxy)quinolin-4-yl]-7-bromo-2,3,4,5-tetrahydro-1,4-benzoxazepineHCID 6681998070,4%

Reaktionsschritte

A mixture of commercially available 4-chloro-6,7-dimethoxyquinoline (120 mg, 0.53 mmol), 7-bromo-2,3-dihydro-1,4-benzoxazepine hydrochloride (example 2, step 1) (200 mg, 0.53 mmol), diisopropylethylamine (0.14 g, 1.1 mmol), in NMP (2 mL) was stirred in a microwave reactor at 120° C. for 45 min. After cooling to room temperature, the reaction mixture was purified directly by silica gel flash chromatography (0-10% methanol-dichloromethane gradient) to give 4-[6,7-bis(methyloxy)quinolin-4-yl]-7-bromo-2,3,4,5-tetrahydro-1,4-benzoxazepine (155 mg, 70% yield), MS (EI) for C20H19N2O3: 415 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08648066B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-07673876c26f4e7081bfe0b2a7a8501e
Quellennotizuspto-grants-2014_02