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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 39266Erstellt: 23. Oktober 2026

Alendronic Acid → HCID 87302179, Verbindung

https://huagongshe.com/de/reaction/39266

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAlendronic AcidHCID 2088—
EduktDimethylformamideHCID 6228—
EduktDiisopropylethylamineHCID 81531—
EduktMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
EduktGlycyl-phenylalanyl-glycineHCID 6992441—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 87302179HCID 87302179—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of bisphosphonate 8 (400 mg, 0.98 mmol) in DMF (5 mL) at 0° C. was added DIEA (341 μL, 1.96 mmol) and HBTU (372 mg, 0.98 mmol). After stirring for 10 min at 0° C., the resulting activated ester solution was added to crude tripeptide 75 (0.98 mmol) and stirring was pursued for 2.5 h at 0° C. The reaction mixture was diluted with ethyl acetate, washed with H2O, 1N HCl solution, saturated NaHCO3 solution and saturated NaCl solution. The organic layer was dried over MgSO4, filtered and concentrated to dryness. The crude product was purified by silica gel chromatography on a Biotage™ flash chromatography system using a gradient of 0-10% methanol in ethyl acetate. Compound 76 was obtained as a colorless gum (652 mg, 92%). 1H NMR (400 MHz, CDCl3) δ 1.44 (s, 9H), 2.22-2.37 (m, 2H), 2.57 (t, J=6.4 Hz, 2H), 2.62 (tt, J=23.9, 7.0 Hz, 1H), 3.03-3.09 (m, 1H), 3.14-3.20 (m, 1H), 3.77-3.93 (m, 4H), 4.58-4.63 (m, 8H), 4.66-4.71 (m, 1H), 5.21-5.26 (m, 4H), 5.33-5.41 (m, 4H), 5.89-5.99 (m, 4H), 6.58-6.66 (m, 2H), 7.09 (d, J=8.2, 1H), 7.19-7.23 (m, 3H), 7.27-7.30 (m, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524691B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-ff1ade8889734ef28619030a99ed52be
Quellennotizuspto-grants-2013_09