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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(3R)-3-amino-3-phenylpropanoic acidHCID 686703—
EduktSodium MethoxideHCID 10942334—
EduktHCID 89812860HCID 89812860—
Lösungsmittel2-MethoxyethanolHCID 8019—
Produkt(R)-3-[(1-Cyano-4-hydroxy-7-phenoxy-isoquinoline-3-carbonyl)-amino]-3-phenyl-propionic acidHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09409892B2
Quelldatensatzuspto-grants-2016_08
ORD IDord-11613c29fc154c42b7661b7bd0258354
Quellennotizuspto-grants-2016_08