HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1481028Erstellt: 25. Oktober 2026
(3R)-3-amino-3-phenylpropanoic acid → (R)-3-[(1-Cyano-4-hydroxy-7-phenoxy-isoquinoline-3-carbonyl)-amino]-3-phenyl-propionic acid
https://huagongshe.com/reaction/1481028
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | (3R)-3-amino-3-phenylpropanoic acid | HCID 686703 | — |
| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Edukt | HCID 89812860 | HCID 89812860 | — |
| Lösungsmittel | 2-Methoxyethanol | HCID 8019 | — |
| Produkt | (R)-3-[(1-Cyano-4-hydroxy-7-phenoxy-isoquinoline-3-carbonyl)-amino]-3-phenyl-propionic acid | HCID 71737525 | — |
Reaktionsschritte
Methyl 1-cyano-4-hydroxy-7-phenoxyisoquinoline-3-carboxylate (20 mg, 0.06 mmol), (R)-3-amino-3-phenyl-propionic acid (62 mg, 0.38 mmol, PepTech) and sodium methoxide (19 mg, 0.35 mmol) were suspended in 2-methoxyethanol (3 mL). The resulting mixture was heated to reflux for 3 hours and then cooled to room temperature. The solvent was removed in vacuo and the residue was dissolved in H2O (15 mL) and EtOAc (15 mL). To the stirred mixture was added 1 N hydrochloric acid until pH was 1. The layers were separated and the aqueous layer was extracted twice with EtOAc. The combined organic layers were dried over MgSO4, concentrated, and purified by flash chromatography (0-50% EtOAc/CH2Cl2 with 0.5% formic acid) to give the title compound in 17 mg. MS: (−) m/z 451.93 (M−1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09409892B2 |
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| Quelldatensatz | uspto-grants-2016_08 |
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| ORD ID | ord-11613c29fc154c42b7661b7bd0258354 |
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| Quellennotiz | uspto-grants-2016_08 |
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