HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Methanol → (S)-1,3,4,5-Tetrahydro-4-amino-3-oxo-2 H-2-benzazepine-2-acetic acid, ethyl ester
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | Chloroform | HCID 6212 | — |
| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | (S)-1,3,4,5-tetrahydro-4-[[(phenylmethoxy)carbonyl]amino]-3-oxo-2H-2-benzazepine-2-acetic acid, ethyl ester | HCID 86749789 | — |
| Katalysator | Palladium hydroxide | HCID 9942167 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | (S)-1,3,4,5-Tetrahydro-4-amino-3-oxo-2 H-2-benzazepine-2-acetic acid, ethyl ester | HCID 86749788 | — |
Reaktionsschritte
20% Palladium hydroxide/carbon catalyst was added to a solution of (S)-1,3,4,5-tetrahydro-4-[[(phenylmethoxy)carbonyl]amino]-3-oxo-2H-2-benzazepine-2-acetic acid, ethyl ester (1.037 g., 2.62 mmole) in absolute ethanol (20 ml.) and the resulting suspension was stirred under a hydrogen atmosphere (balloon) for 2 hours. The mixture was filtered through Celite and filtrate was evaporated to dryness. The semi-solid residue was triturated with hexane to give 0.63 g. of product as a white, crystalline solid; m.p. 71°-73° C.; Rf =0.38 (methanol:methylene chloride, 1:9); [α]D =77.5° (c=0.59, chloroform).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05723602 |
| Quelldatensatz | uspto-grants-1998_03 |
| ORD ID | ord-d232c1adede245b1b40453d6829ded7a |
| Quellennotiz | uspto-grants-1998_03 |