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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022713Generated: October 29, 2026

Acetone → HCID 178434042, compound

https://huagongshe.com/reaction/1022713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantAcetohydrazideHCID 14039—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-butyl (6R,7R)-6-(2-amino-2-thioxoethyl)-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylateHCID 86663871—
ProductHCID 178434042HCID 17843404279%

Reaction Steps

Methyl iodide (0.214 mL, 3.43 mmol) was added to a suspension of tert-butyl (6R,7R)-6-(2-amino-2-thioxoethyl)-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylate (288 mg, 0.69 mmol) and potassium carbonate (142 mg, 1.03 mmol) in acetone (5 mL) at room temperature. The reaction mixture was stirred at room temperature for 4 hr, and concentrated under reduced pressure. To the residue was added aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was dissolved in toluene (5 ml), acetohydrazide (61.1 mg, 0.82 mmol) was added, and the mixture was stirred at 120° C. overnight while using a Dean-Stark trap. To the reaction mixture was added aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (241 mg, 0.545 mmol, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722662B2
Source datasetuspto-grants-2014_05
ORD IDord-0dc2c02fac124c96bbb19acd3b653633
Source noteuspto-grants-2014_05