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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantSulfuric AcidHCID 1118—
ReactantSodium BicarbonateHCID 516892—
Reactant2-[2-(7-Chloroquinolin-4-ylamino)ethoxy]ethanolHCID 53360452—
SolventWaterHCID 962—
Product[2-(2-Bromoethoxy)ethyl]-(7-chloroquinolin-4-yl)amineHCID 6719044831%

Reaction Conditions

Temperature155 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947701B2
Source datasetuspto-grants-2011_05
ORD IDord-3c3c8de9b9964bd393066ef0795e29ac
Source noteuspto-grants-2011_05