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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514248Generated: November 2, 2026

Ethyl 3-bromopropionate → Ethyl 3-[9-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1,4-benzoxazepin-4(5H)-yl]propanoate

https://huagongshe.com/reaction/1514248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-bromopropionateHCID 68320—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 68468994HCID 68468994—
SolventAcetonitrileHCID 6342—
ProductEthyl 3-[9-(5-{3-cyano-4-[(1-methylethyl)oxy]phenyl}-1,2,4-oxadiazol-3-yl)-2,3-dihydro-1,4-benzoxazepin-4(5H)-yl]propanoateHCID 5940354338.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 2-[(1-methylethyl)oxy]-5-[3-(2,3,4,5-tetrahydro-1,4-benzoxazepin-9-yl)-1,2,4-oxadiazol-5-yl]benzonitrile hydrochloride (Example 32) (90 mg, 0.218 mmol) in acetonitrile (10 ml) was added N,N-diisopropylethylamine (0.076 ml, 0.436 mmol) followed by ethyl 3-bromopropanoate (0.056 ml, 0.436 mmol). The reaction mixture was heated at 80° C. overnight. A further 1 equivalent of N,N-diisopropylethylamine and ethyl 3-bromopropanoate were added and heating continued overnight. The reaction mixture was cooled and evaporated. Purification of the residue by column chromatography on silica, eluting with 60-70% ethyl acetate in cyclohexane to give the title compound as a brown oil (40 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222245B2
Source datasetuspto-grants-2012_07
ORD IDord-fbcbcb55f29b4cdf88f62918045e96bc
Source noteuspto-grants-2012_07