HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 448644Erstellt: 24. Oktober 2026
Hydrochloric Acid → (2S,4R)-4-amino-5-biphenyl-4-yl-2-hydroxymethyl-2-methyl-pentanoic acid 1-cyclohexyloxycarbonyloxy-ethyl ester
https://huagongshe.com/de/reaction/448644
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 1,4-Dioxane | HCID 31275 | — |
| Edukt | 1-Chloroethyl Cyclohexyl Carbonate | HCID 11229529 | — |
| Edukt | (2S,4R)-5-Biphenyl-4-yl-4-t-butoxycarbonylamino-2-hydroxymethyl-2-methyl-pentanoic acid | HCID 68181022 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | (2S,4R)-4-amino-5-biphenyl-4-yl-2-hydroxymethyl-2-methyl-pentanoic acid 1-cyclohexyloxycarbonyloxy-ethyl ester | HCID 68181297 | — |
Reaktionsschritte
1-Chloroethyl cyclohexyl carbonate (240 mg, 1.2 mmol) was added to a mixture of (2S,4R)-5-biphenyl-4-yl-4-t-butoxycarbonylamino-2-hydroxymethyl-2-methyl-pentanoic acid (300 mg, 726 μmol) and Et3N (106 μL, 762 μmol) in acetone (10 mL). The mixture was refluxed for 24 hours and the reaction monitored for completion. The individual isomers were separated (˜1:1) and purified (Interchim reverse phase chromatography column) the solvent was removed under vacuum. MeCN (2 mL) and 4 M HCl in 1,4-dioxane (3 mL, 10 mmol) was added and the resulting mixture was stirred for 30 minutes. The solvent was evaporated under vacuum and the product was azeotroped with toluene (1×) to yield (2S,4R)-4-amino-5-biphenyl-4-yl-2-hydroxymethyl-2-methyl-pentanoic acid 1-cyclohexyloxycarbonyloxy-ethyl ester.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08481044B2 |
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| Quelldatensatz | uspto-grants-2013_07 |
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| ORD ID | ord-408832e6487f40b8ad3a0e4872f6cecf |
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| Quellennotiz | uspto-grants-2013_07 |
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