HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Sodium borohydride → (2S,5R)-5-[(1S,2S)-2-Amino-3-(3,5-difluoro-phenyl)-1-hydroxypropyl]-2-ethoxymorpholine-4-carboxylic acid tert-butyl ester
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | (2S,5R)-5-[(1R,2S)-3-(3,5-difluorophenyl)-1-hydroxy-2-nitropropyl]-2-ethoxymorpholine-4-carboxylic acid tert-butyl ester | HCID 68561117 | — |
| Katalysator | Nickel Dichloride | HCID 24385 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | (2S,5R)-5-[(1S,2S)-2-Amino-3-(3,5-difluoro-phenyl)-1-hydroxypropyl]-2-ethoxymorpholine-4-carboxylic acid tert-butyl ester | HCID 68562756 | 70,2% |
Reaktionsschritte
Add sodium borohydride (0.061 g, 1.62 mmol) portionwise to a solution of (2S,5R)-5-[(1R,2S)-3-(3,5-difluorophenyl)-1-hydroxy-2-nitropropyl]-2-ethoxymorpholine-4-carboxylic acid tert-butyl ester (0.145 g, 0.325 mmol) and nickel (II) chloride (0.063 g, 0.487 mmol) at room temperature in methanol (5 mL) and stir 30 for min. Add water (˜3 mL) and concentrate. Dilute with ethyl acetate and filter through a filtering agent. Partition the filtrate between ethyl acetate and water, dry (magnesium sulfate) and concentrate to give the title compound as a white solid (95 mg, 70%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07745438B2 |
| Quelldatensatz | uspto-grants-2010_06 |
| ORD ID | ord-c600e7253e0e4dd79af57879c261dd45 |
| Quellennotiz | uspto-grants-2010_06 |