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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514232Generated: November 2, 2026

Potassium Iodide → Ethyl 4-[9-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1,4-benzoxazepin-4(5H)-yl]butanoate

https://huagongshe.com/reaction/1514232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 4-bromobutyrateHCID 76300—
Reactant9-(5-{3-Chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-2,3,4,5-tetrahydro-1,4-benzoxazepine hydrochlorideHCID 68465494—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductEthyl 4-[9-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1,4-benzoxazepin-4(5H)-yl]butanoateHCID 59403438—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 9-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-2,3,4,5-tetrahydro-1,4-benzoxazepine hydrochloride (Example 31) (20 g, 47.4 mmol), potassium carbonate (16.4 g, 118 mmol) and potassium iodide (7.86 g, 47.4 mmol) in N,N-dimethylformamide (DMF) (250 ml) was treated with ethyl 4-bromobutanoate (7.46 ml, 52.1 mmol) and the resulting mixture stirred at 80° C. under nitrogen for 180 minutes. The mixture was allowed to cool and poured into water (1000 ml). The resulting precipitate was extracted into ethyl acetate (3×250 ml) and the extracts combined, washed with water (2×250 ml), then brine (150 ml), dried (sodium sulphate) and evaporated to give a colourless viscous oil. The crude material was purified by chromatography on silica, eluting with a 20-100% gradient of ethyl acetate in isohexane to give the title compound as a colourless, viscous oil which crystallised on standing (18.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222245B2
Source datasetuspto-grants-2012_07
ORD IDord-41df72a8e3084cf3a5f27f6aee12265c
Source noteuspto-grants-2012_07