HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022604Generated: October 30, 2026
Sodium hydride → tert-butyl (6R,7R)-6-[(3-cyano-2-oxopyridin-1(2H)-yl)methyl]-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylate
https://huagongshe.com/reaction/1022604
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | tert-butyl (6S,7R)-7-(3,4-dichlorophenyl)-6-{[(methylsulfonyl)oxy]methyl}-1,4-oxazepane-4-carboxylate | HCID 86663851 | — |
| Reactant | HCID 178510022 | HCID 178510022 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | tert-butyl (6R,7R)-6-[(3-cyano-2-oxopyridin-1(2H)-yl)methyl]-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylate | HCID 66975537 | 86.2% |
Reaction Steps
60% Sodium hydride (0.086 g) was added to a mixed solution of 3-cyano-2-hydroxypyridine (0.206 g) in 1,2-dimethoxyethane (4 ml)-DMF (2 ml) under ice-cooling, and the mixture was stirred for 5 min. To the reaction solution was added lithium bromide (0.248 g), and the mixture was stirred at room temperature for 0.5 hr. To the reaction solution was added a solution of tert-butyl (6S,7R)-7-(3,4-dichlorophenyl)-6-{[(methylsulfonyl)oxy]methyl}-1,4-oxazepane-4-carboxylate (0.65 g) in 1,2-dimethoxyethane (4 mL), and the mixture was stirred at 60° C. overnight. To the reaction mixture was added water, 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 (0.59 g, 86%).
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-9562f151821a41189674e76f724f7a05 |
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| Source note | uspto-grants-2014_05 |
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