HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022614Generated: November 3, 2026
HCID 66975351, compound → HCID 66975769, compound
https://huagongshe.com/reaction/1022614
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 66975351 | HCID 66975351 | — |
| Reactant | HCID 178482962 | HCID 178482962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 66975769 | HCID 66975769 | 116.4% |
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
| 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-37677fb1aa474ff8a2d3e20b29c7dbcc |
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| Source note | uspto-grants-2014_05 |
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