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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022727Generated: November 2, 2026

Methyl iodide → tert-butyl (6R,7S)-7-(3,4-dichlorophenyl)-6-(methylamino)-1,4-oxazepane-4-carboxylate

https://huagongshe.com/reaction/1022727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactanttert-butyl (6R,7S)-6-amino-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylateHCID 66975508—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Producttert-butyl (6R,7S)-7-(3,4-dichlorophenyl)-6-(methylamino)-1,4-oxazepane-4-carboxylateHCID 66976611—

Reaction Steps

To a solution of tert-butyl (6R,7S)-6-amino-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylate (150 mg) in THF (4 mL) was added methyl iodide (0.026 ml) at room temperature, and the mixture was stirred at room temperature overnight. The reaction mixture was diluted with ethyl acetate. The diluted solution was washed with distilled water and brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel chromatography (hexane/ethyl acetate) to give the title compound (30 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722662B2
Source datasetuspto-grants-2014_05
ORD IDord-de40324e5da84666a0140abdb3d79239
Source noteuspto-grants-2014_05