HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022555Generated: November 1, 2026
HCID 66975023, compound → HCID 66975423, compound
https://huagongshe.com/reaction/1022555
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 66975023 | HCID 66975023 | — |
| Reactant | HCID 178482962 | HCID 178482962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 66975423 | HCID 66975423 | 117.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722662B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-2ebfa3c419214a4d9a43827af3376cb1 |
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| Source note | uspto-grants-2014_05 |
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