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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | 1-(3,4-dihydro-1H-isoquinolin-2-yl)-2-isobutylamino-ethanone | HCID 22498787 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-bromo-N-[2-(3,4-dihydro-1H-isoquinolin-2-yl)-2-oxo-ethyl]-N-isobutyl-acetamide | HCID 22498791 | 51.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06878706B1 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-3e0dd3305ade46019a2f473107d904c6 |
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| Source note | uspto-grants-2005_04 |
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