HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ammonium cerium (IV) nitrate → (3aR*,10aS*)-4-(phthalimidoacetyl)-9-(3,5,6-trimethyl-1,4-benzoquinon-2-ylmethyl)-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-one
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ammonium cerium (IV) nitrate | HCID 9869224 | — |
| Edukt | HCID 86753321 | HCID 86753321 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | (3aR*,10aS*)-4-(phthalimidoacetyl)-9-(3,5,6-trimethyl-1,4-benzoquinon-2-ylmethyl)-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-one | HCID 70111246 | 63,2% |
Reaktionsschritte
In a mixture of acetonitrile (3 mL) and water (2 mL) was suspended (3aR*,10aS*)-9-(2,5-dimethoxy-3,4,6-trimethylbenzyl)-4-(phthalimidoacetyl)-2,3,3a,4,9,10a-hexahydrobenzo[b]cyclopenta[e][1,4]diazepin-10(1H)-one (0.5 g, 0.86 mmol). To the suspension was added, while stirring, a solution of ammonium cerium (IV) nitrate (1.4 g, 2.55 mmol) in a mixture of acetonitrile (2 mL) and water (2 mL). The reaction mixture was stirred for one hour, which was diluted with water, followed by extraction with chloroform. The extract was washed with water and dried, then the solvent was distilled off. The residue was crystallized from ethyl acetate to give 300 mg (yield 63%) of the titled compound, m.p. 258°-260° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05834463 |
| Quelldatensatz | uspto-grants-1998_11 |
| ORD ID | ord-847abb0f88834618ac59ca324403a869 |
| Quellennotiz | uspto-grants-1998_11 |