HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1184045Erstellt: 26. Oktober 2026
Benzyl N-[(1S)-2-[(1S,3S,5S)-3-cyano-2-azabicyclo[3.1.0]hexan-2-yl]-1-(3-hydroxyadamantan-1-yl)-2-oxo ethyl]carbamate → Saxagliptin
https://huagongshe.com/reaction/1184045
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Benzyl N-[(1S)-2-[(1S,3S,5S)-3-cyano-2-azabicyclo[3.1.0]hexan-2-yl]-1-(3-hydroxyadamantan-1-yl)-2-oxo ethyl]carbamate | HCID 86703399 | — |
| Katalysator | Palladium | HCID 23938 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | Saxagliptin | HCID 11243969 | — |
Reaktionsschritte
To a solution of benzyl N-[(1S)-2-[(1S,3S,5S)-3-cyano-2-azabicyclo[3.1.0]hexan-2-yl]-1-(3-hydroxyadamantan-1-yl)-2-oxo-ethyl]carbamate (10 gm) of formula-IX in acetonitrile, 5% Pd/C (50% wet, 1 gm) was added. Hydrogen gas was bubbled through the reaction mass for 4 hrs at 20-25° C. After complete conversion of starting material, the reaction mass was filtered. The filtrate was evaporated to yield SAXAGLIPTIN free base of formula-I as a foamy solid. To the solid ethyl acetate (5 ml), 20 micro liters of water and n-hexane (20 ml) were added, the mixture stirred at 0-5° C. and the white solid formed was filtered to yield 7.06 gm (95%) of SAXAGLIPTIN MONO HYDRATE of formula-XII. The solid obtained was dissolved in ethyl acetate (30 ml), 2.15 ml of concentrated hydrochloric acid added at 20-25° C., stirred for one hour and the white solid formed was filtered to yield saxagliptin dihydrate mono-hydrochloride of formula-II.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08664443B2 |
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| Quelldatensatz | uspto-grants-2014_03 |
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| ORD ID | ord-2100f039bdb9423c9d19dca764e87e57 |
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| Quellennotiz | uspto-grants-2014_03 |
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