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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1827259Erstellt: 25. Oktober 2026

Glycine → HCID 178491777, Verbindung

https://huagongshe.com/reaction/1827259

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktGlycineHCID 750—
EduktD-PhenylalanineHCID 71567—
EduktN-Methyl-L-valineHCID 444080—
Edukt4-tert-Butyl hydrogen L-aspartateHCID 7010570—
EduktTrifluoroacetic acid methylene chlorideHCID 21863450—
EduktHCID 178491778HCID 178491778—
EduktHCID 178491779HCID 178491779—
ProduktHCID 178491777HCID 178491777—

Reaktionsschritte

Fmoc-Arg(Mtr)-Gly-Asp(OBut)-DPhe-NMeVal-ONa (SEQ ID NO 41) is synthesized using solid-phase Merrifield-type procedures by sequentially adding NMeVal, DPhe, Asp(OBut), Gly and Fmoc-Arg(Mtr) in a step-wise manner to a 4-hydroxymethyl-phenoxymethyl-polystyrene resin (Wang type resin) (customary Merrifield-type methods of peptide synthesis are applied as described in Houben-Weyl, l.c., Volume 15/II, Pages 1 to 806 (1974). The polystyrene resin and amino acid residues precursors are commercially available from Aldrich, Sigma or Fluka chemical companies). After completion of sequential addition of the amino acid residues, the resin is then eliminated from the peptide chain using a 1:1 mixture of TFA/dichloromethane which provides the Fmoc-Arg(Mtr)-Gly-Asp(OBut)-DPhe-NMeVal-OH product (SEQ ID NO 42). The Fmoc group is then removed with a 1:1 mixture of piperidine/DMF which provides the crude Arg(Mtr)-Gly-Asp(OBut)-DPhe-NMeVal-OH (SEQ ID NO 43) precursor which is then purified by HPLC in the customary manner.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07053041B1
Quelldatensatzuspto-grants-2006_05
ORD IDord-8a1f3e9205a64558bb261b5185b2c6ca
Quellennotizuspto-grants-2006_05