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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38025Generated: October 26, 2026

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

https://huagongshe.com/reaction/38025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDipropylamineHCID 8902—
ReactantPotassium Sodium TartrateHCID 9357—
ReactantTrimethylaluminumHCID 16682925—
Reactantethyl 2-amino-8-bromo-3H-benzo[b]azepine-4-carboxylateHCID 58228535—
SolventTolueneHCID 1140—
Product(1E,4E)-2-amino-8-bromo-N,N-dipropyl-3H-benzo[b]azepine-4-carboxamideHCID 6696144634.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524702B2
Source datasetuspto-grants-2013_09
ORD IDord-febcc2bbf55a49ebae7f0dc6f20e7b7e
Source noteuspto-grants-2013_09