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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 450214Erstellt: 26. Oktober 2026

5-Hydroxyindole → 1H-Indole, 5-[[6-[(phenylmethoxy)methyl]-4-pyrimidinyl]oxy]-

https://huagongshe.com/reaction/450214

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-HydroxyindoleHCID 16054—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Edukt4-((Benzyloxy)methyl)-6-chloropyrimidineHCID 53421259—
LösungsmittelAcetonitrileHCID 6342—
Produkt1H-Indole, 5-[[6-[(phenylmethoxy)methyl]-4-pyrimidinyl]oxy]-HCID 59394260—

Reaktionsschritte

To a solution of 5-hydroxy indole (1.33 g, 10 mmol) and 4-benzyloxymethyl-6-chloro-pyrimidine (2.35 g, 10 mmol) in acetonitrile (20 mL) is added DBU. After 16 h at rt the solution is concentrated under reduced pressure. The residue is purified by FCC (EtOAc/Heptane from 0% to 40%) to give 5-(6-benzyloxymethyl-pyrimidin-4-yloxy)-1H-indole. MS (ESI) m/z 447.0 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08486954B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-d14caae172fa4d15a7071c440b946bd1
Quellennotizuspto-grants-2013_07