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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 629720Erstellt: 25. Oktober 2026

Methanol → tert-butyl (2R,5R)-5-(azidomethyl)-2-[2-(2-{[N-(methoxycarbonyl)-beta-phenyl-L-phenylalanyl]amino}phenyl)ethyl]morpholine-4-carboxylate

https://huagongshe.com/reaction/629720

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktSodium BicarbonateHCID 516892—
EduktMethanesulfonyl azide, trifluoro-HCID 10986786—
Edukttert-butyl (2R,5R)-5-(aminomethyl)-2-[2-(2-{[N-(methoxycarbonyl)-beta-phenyl-L-phenylalanyl]amino}phenyl)ethyl]morpholine-4-carboxylateHCID 86726318—
KatalysatorCopper SulfateHCID 24462—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkttert-butyl (2R,5R)-5-(azidomethyl)-2-[2-(2-{[N-(methoxycarbonyl)-beta-phenyl-L-phenylalanyl]amino}phenyl)ethyl]morpholine-4-carboxylateHCID 86726323—

Reaktionsschritte

To a solution of tert-butyl (2R,5R)-5-(aminomethyl)-2-[2-(2-{[N-(methoxycarbonyl)-β-phenyl-L-phenylalanyl]amino}phenyl)ethyl]morpholine-4-carboxylate (1 eq.) in CH2Cl2 (0.4M) was added copper(II) sulfate (0.02 eq.) and sodium bicarbonate (1 eq.) as a solution in water (NaHCO3/CuSO4)) (1M). To that mixture was added triflic azide (3.65 eq.) as a solution in CH2Cl2 (0.4M). The heterogenous mixture was homogenized by the addition of methanol and the reaction was stirred at room temperature for 30 minutes. Upon completion by LCMS, solvents were evaporated and the evaporation residue was used as such for next step.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09315475B2
Quelldatensatzuspto-grants-2016_04
ORD IDord-c2ea0a96f46c46179bbcc94fdf00c96a
Quellennotizuspto-grants-2016_04