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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 731520Erstellt: 24. Oktober 2026

Hydrochloric Acid → HCID 131727621, Verbindung

https://huagongshe.com/de/reaction/731520

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt4-MethylmorpholineHCID 7972—
EduktDiisopropylcarbodiimideHCID 12734—
Edukt1-HydroxybenzotriazoleHCID 75771—
EduktN2-((tert-Butoxy)carbonyl)-L-asparagineHCID 82035—
EduktTert-butyl (2S)-2-amino-3-[4-(tert-butoxy)phenyl]propanoateHCID 7350495—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 131727621HCID 131727621—

Reaktionsschritte

Boc-Asn-OH (3.5 g 15 mmol) is dissolved in dichloromethane (100 ml amylene stabilised free of alcohol) and HOBt (2.24 g dry 16.5 mmol) is added. The mixture is cooled in an ice/water bath and DIC (2.45 ml 16 mmol) is added. The mixture will be allowed to react for 20 min. The HOBt on the bottom will react and a precipitate of DIU (on top) will form. H-Tyr(tBu)-OtBu×HCl (5.1 g 15.4 mmol) is dissolved in DMF (30 ml dry). The dichloromethane mixture containing the activated ester is filtered from the DIU directly into the DMF solution. The combined mixture is cooled in ice/water and NMM (1.75 ml 15.8 mmol) is added. The mixture is allowed to react over night. The solvents will be removed in vacuo. Ethyl acetate 200 ml is added and a precipitate is removed and the solution is washed with citric acid (2×50 ml 10%), sodium hydrogen carbonate (2×50 ml saturated) and brine (2×50 ml). The solution is dried with magnesium sulfate and the solvent removed in vacuo ending at 0.2 mBar for 30 min. The raw product will be suspended in pentane (40 ml) and filtered from a precipitate of DIU. The pentane will be removed in vacuo yielding the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07585839B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-149181ff9f0b411ab915340f7bedcfde
Quellennotizuspto-grants-2009_09