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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022555Generated: November 1, 2026

HCID 66975023, compound → HCID 66975423, compound

https://huagongshe.com/reaction/1022555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66975023HCID 66975023—
ReactantHCID 178482962HCID 178482962—
SolventAcetonitrileHCID 6342—
ProductHCID 66975423HCID 66975423117.6%

Reaction Steps

To a solution of tert-butyl (6RS,7RS)-6-(aminomethyl)-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylate (144 mg) in acetonitrile (2 mL) was added N-(tert-butoxycarbonyl)-N-[4-(dimethylazaniumylidene)-1,4-dihydropyridin-1-ylsulfonyl]azanide (190 mg) prepared by the method described in Organic Letters, 2001, 3 (14), 2241-2243, and the mixture was stirred at room temperature for 20 hr. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with ethyl acetate. The diluted solution was washed with 1 N hydrochloric acid and brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel chromatography (hexane/ethyl acetate) to give the title compound (205 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722662B2
Source datasetuspto-grants-2014_05
ORD IDord-2ebfa3c419214a4d9a43827af3376cb1
Source noteuspto-grants-2014_05