Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814737Generated: October 30, 2026

Bromoacetyl bromide → 2-bromo-N-[2-(3,4-dihydro-1H-isoquinolin-2-yl)-2-oxo-ethyl]-N-isobutyl-acetamide

https://huagongshe.com/reaction/1814737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl bromideHCID 61147—
Reactant1-(3,4-dihydro-1H-isoquinolin-2-yl)-2-isobutylamino-ethanoneHCID 22498787—
SolventTetrahydrofuranHCID 8028—
Product2-bromo-N-[2-(3,4-dihydro-1H-isoquinolin-2-yl)-2-oxo-ethyl]-N-isobutyl-acetamideHCID 2249879151.4%

Reaction Steps

To a stirred solution of 1-(3,4-dihydro-1H-isoquinolin-2-yl)-2-isobutylamino-ethanone (0.45 g, 1.8 mmol) in THF (4.0 mL), a solution of bromoacetyl bromide (0.32 mL, 3.6 mmol) in 4.0 mL THF was added dropwise at −78° C., under argon. After 3 h (the temperature gradually rose to 10° C.) the reaction was concentrated and the remaining residue was diluted with methylene chloride and saturated NaHCO3. The layers were separated and the organic phase was washed with brine and then dried (MgSO4). Filtration and concentration gave the crude product which was purified via silica gel flash chromatography (0-5% MeOH/methylene chloride, 30 mL/min.) to give 0.34 g (51%) of 2-bromo-N-[2-(3,4-dihydro-1H-isoquinolin-2-yl)-2-oxo-ethyl]-N-isobutyl-acetamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878706B1
Source datasetuspto-grants-2005_04
ORD IDord-3e0dd3305ade46019a2f473107d904c6
Source noteuspto-grants-2005_04