Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanesulfonyl chloride | HCID 31297 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | (1S,3S,5S)-2-Azabicyclo[3.1.0]hexane-3-carboxamide hydrochloride | HCID 11564521 | — |
| Edukt | (2S)-((tert-Butoxycarbonyl)amino)(3-hydroxytricyclo(3.3.1.1 3,7)dec-1-yl)acetic acid | HCID 11723843 | — |
| Edukt | HCID 178418300 | HCID 178418300 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Boc-saxagliptin | HCID 51358360 | — |
Reaktionsschritte
A 2 L three-necked flask equipped with a thermometer, a mechanical stirrer and a gas inlet was charged with (αS)-α[[(1,1-dimethylethoxy)carbonyl]amino]-3-hydroxytricyclo[3.3.1.13,7]decane-1-acetic acid (Formula 3) (50 grams, 153.8 mmol). THF (200 ml) was added and stirred to produce a clear solution. The solution was cooled to −6° C. in an acetone-dry ice-water bath. Methanesulfonyl chloride (Mes-Cl) (13.1 ml, 169 mmol, 1.1 equivalents) was then added as a single portion followed by diisopropylethylamine (94 ml, 539 mmol, 1.1 equivalents). The diisopropylethylamine was added slowly over a period of about 4 minutes to keep the internal temperature below 8° C. The reaction mixture was stirred at 0° C. until all acid was converted to mixed anhydride. (1S,3S,5S)-2-azabicyclo[3.1.0]hexane-3-carboxamide hydrochloride salt (32.5 grams, 200 mmol, 1.1 equivalents) and hydroxybenzotriazole (HOBT) (1.04 grams, 7.6 mmol, 0.05 equivalents) were then added in a single portion and the flask was removed from the cooling bath. The reaction mixture was stirred at room temperature for 2 hours and then left overnight at room temperature.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07741082B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-0538aae722e14b908383f853c6c8fd6d |
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| Quellennotiz | uspto-grants-2010_06 |
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