HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 409034Erstellt: 26. Oktober 2026
Lithium borohydride → (5S,6S,9R)-6-(2,3-difluorophenyl)-9-(triisopropylsilyloxy)-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-5-ol
https://huagongshe.com/reaction/409034
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Lithium borohydride | HCID 4148881 | — |
| Edukt | (6S,9R)-6-(2,3-Difluorophenyl)-6,7,8,9-tetrahydro-9-[[tris(1-methylethyl)silyl]oxy]-5H-cyclohepta[b]pyridin-5-one | HCID 57911475 | — |
| Lösungsmittel | Cyclopentyl methyl ether | HCID 138539 | — |
| Produkt | (5S,6S,9R)-6-(2,3-difluorophenyl)-9-(triisopropylsilyloxy)-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-5-ol | HCID 57911423 | 65% |
Reaktionsschritte
Lithium borohydride (0.982 g, 45.1 mmol) was added to a cyclopentyl methyl ether (30 mL) solution of (6S,9R)-6-(2,3-difluorophenyl)-9-(triisopropylsilyloxy)-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-5-one (5.0224 g, 11.27 mmol) at 0° C. under N2. The reaction mixture was stirred at 0° C. for 2 hours and then an addition 4 hours at room temperature. The reaction was quenched by adding methanol. The reaction mixture was stirred for 0.5 hour. The solvent was mostly removed via vacuum and the crude material was taken up in ethyl acetate, which was washed with water three times. Flash column by ethyl acetate in hexane from 0 to 10% gave the desired product (3.28 g, 65%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08759372B2 |
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| Quelldatensatz | uspto-grants-2014_06 |
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| ORD ID | ord-613adbb88c844232aca16582d503ae0a |
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| Quellennotiz | uspto-grants-2014_06 |
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