Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 539506Erstellt: 26. Oktober 2026

Carbamate → (Quinolin-3-yl)methanol

https://huagongshe.com/reaction/539506

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbamateHCID 276—
EduktQuinolineHCID 7047—
EduktSodium borohydrideHCID 4311764—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(Quinolin-3-yl)methanolHCID 12662983—

Reaktionsschritte

Synthesis of compounds ERW1041A, B, C, D, E, and 1069 were synthesized using the methods of Choi et al. Chemistry & Biology, Volume 12, Issue 4, Pages 469-475, except the amino-acid amines are protected by a quinoline-containing carbamate. This quinoline-containing carbamate is synthesized by reducing 3-quinolylcarbaldehyde with sodium borohydride in THF followed by an aqueous workup and flash chromatography yielding 3-quinolylcarbinol. para-Nitro-phenylchloroformate is reacted with 3-quinolylcarbinol in methylene chloride and N-methyl morpholine to give a carbonate of 3-quinoline methanol and para-Nitro-phenol. After purification by flash chromatography, this carbonate is reacted with the methyl ester of the amino acid in neat DMF to give the named compounds.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08871718B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-081ecec58c714981b4aae8a58db36932
Quellennotizuspto-grants-2014_10