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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022614Generated: November 3, 2026

HCID 66975351, compound → HCID 66975769, compound

https://huagongshe.com/reaction/1022614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66975351HCID 66975351—
ReactantHCID 178482962HCID 178482962—
SolventAcetonitrileHCID 6342—
ProductHCID 66975769HCID 66975769116.4%

Reaction Steps

To a solution of tert-butyl (6R,7R)-6-(aminomethyl)-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylate (100 mg) in acetonitrile (2 mL) was added N-(tert-butoxycarbonyl)-N-[4-(dimethylazaniumylidene)-1,4-dihydropyridin-1-ylsulfonyl]azanide (181 mg) prepared by the method described in Organic Letters, 2001, 3 (14), 2241-2243, and the mixture was stirred at room temperature for 12 hr. The reaction mixture was concentrated under reduced pressure, distilled water was added to the residue, and the mixture was extracted twice with ethyl acetate. The combined organic layers were washed with 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 (172 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722662B2
Source datasetuspto-grants-2014_05
ORD IDord-37677fb1aa474ff8a2d3e20b29c7dbcc
Source noteuspto-grants-2014_05