HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550887Generated: October 25, 2026
Hydrogen Bromide → [2-(2-Bromoethoxy)ethyl]-(7-chloroquinolin-4-yl)amine
https://huagongshe.com/reaction/550887
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-[2-(7-Chloroquinolin-4-ylamino)ethoxy]ethanol | HCID 53360452 | — |
| Solvent | Water | HCID 962 | — |
| Product | [2-(2-Bromoethoxy)ethyl]-(7-chloroquinolin-4-yl)amine | HCID 67190448 | 31% |
Reaction Steps
Hydrobromic acid (5.9 ml, 109.1 mmol) and then sulphuric acid (2.0 ml, 37.0 mmol) are added dropwise to 4.7 g of compound 21 (17.6 mmol), the reaction medium being refrigerated using a bath of cold water. The reaction medium is then heated at 155° C. for 2 h 30 min, and then poured into 70 ml of cold water. The pH is then adjusted by adding NaHCO3 (pH approximately 9), and the medium is then extracted at the reflux of toluene (70 ml) for 20 min. The organic phase is then collected and the compound 22 is obtained after crystallization at −18° C. overnight, filtration, washing with hexane, and then drying under vacuum: 1.77 g (yield=31%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07947701B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-3c3c8de9b9964bd393066ef0795e29ac |
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| Source note | uspto-grants-2011_05 |
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