HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Benzylhydroxylamine → HCID 86757319, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Benzylhydroxylamine | HCID 102313 | — |
| Reactant | O-(Tetrahydropyran-2-yl)hydroxylamine | HCID 5142091 | — |
| Reactant | HCID 88228501 | HCID 88228501 | — |
| Product | HCID 86757319 | HCID 86757319 | — |
Reaction Steps
In an analogous manner to that described in Example 1, parts (vi)-(viii), but using (E)-2(R)-[1(S)-(tert-butoxycarbonyl)-4-phenyl-3-butenyl]-4-methyl-2′-[(1-methylhydrazinyl)carbamoyl]valerohydrazide and O-benzylhydroxylamine in place of (E)-2(R)-[1(S)-(tert-butoxycarbonyl)-4-phenyl-3-butenyl]-2 ′-glycinyl-4-methylvalerohydrazide and O-(tetrahydro-2H-pyran-2(RS)-yl)hydroxylamine respectively there was obtained 2(R)-[1(S)-(benzyloxycarbamoyl)-4-phenylbutyl]-4-methyl-N-(1-methyl-3,5-dioxo-1,2,4-triazolidin-4-yl)valeramide in the form of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06281363B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-bcccfb787a6e491882de978cfdd2f9a4 |
| Source note | uspto-grants-2001_08 |