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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222299Generated: October 30, 2026

Water → HCID 69255136, compound

https://huagongshe.com/reaction/2222299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2-bromo-N-(4-methylpent-2-yn-4-yl)butyramideHCID 21078406—
Reactant3-Chloroquinolin-6-olHCID 21923126—
SolventDimethylformamideHCID 6228—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 69255136HCID 6925513666.9%

Reaction Steps

To a stirred mixture of 3-chloro-6-hydroxyquinoline (0.130 g) and anhydrous potassium carbonate (0.110 g) in dry N,N-dimethylformamide (3 ml) at 80° C. was added 2-bromo-N-(4-methylpent-2-yn-4-yl) butyramide (0.197 g) and the reaction maintained at this temperature for 6 hours. The brown suspension produced was cooled to ambient temperature, poured into water and extracted with diethyl ether. The extract was washed with water, dried over magnesium sulphate then evaporated under reduced pressure to give a brown gum. The gum was fractionated by chromatography (silica; hexane/ethyl acetate 4:1 by volume) to give 2-(3-chloro-6-quinolinyloxy)-N-(4-methylpent-2-yn-4-yl) butyramide (0.167 g) as a colourless solid, m.p. 105-107° C., 1H NMR (CDCl3) δ: 1.08(3H, t); 1.58 (3H, s); 1.59(3H, s); 1.77(3H, s); 1.99-2.08(2H, m); 4.55(1H, t); 6.37(1H, s); 7.02(1H, d); 7.41(1H, dd); 8.01(1H, d); 8.02(1H, d); 8.70(1H, m); 8.78(1H,m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07371764B2
Source datasetuspto-grants-2008_05
ORD IDord-64c09b06f96244bd95bb1a0ca05489c8
Source noteuspto-grants-2008_05