HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627657Generated: October 30, 2026
HCID 86728125, compound → HCID 86728126, compound
https://huagongshe.com/reaction/627657
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86728125 | HCID 86728125 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86728126 | HCID 86728126 | — |
Reaction Steps
A solution of tert-butyl N-[(11bR)-3,3,4a,11b-tetramethyl-10-nitro-4,4-dioxo-5,6-dihydro-[1]benzoxepino[4,5-b][1,4]thiazin-2-yl]-N-tert-butoxycarbonyl-carbamate (0.076 g, 0.13 mmol) in EtOAc (0.9 ml) and EtOH (0.5 ml) was stirred under hydrogen balloon in the presence of palladium, 10% wt. on activated carbon (0.036 g, 0.033 mmol) for 15 h. The mixture was filtered through the plug of Celite, filter cake was washed with ethyl acetate. The combined filtrate was concentrated to afford crude tert-butyl N-[(11bR)-10-amino-3,3,4a,11b-tetramethyl-4,4-dioxo-5,6-dihydro-[1]benzoxepino[4,5-b][1,4]thiazin-2-yl]-N-tert-butoxycarbonyl-carbamate as mixture of trans and cis diasteromers (˜1:3 ratio) which was used without further purification. m/z (ESI) 560.0 (M+Na)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09309263B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-e5b55f9fb6ed43fdbacdacdcc9ae6160 |
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| Source note | uspto-grants-2016_04 |
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