Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827259Generated: October 26, 2026

Glycine → HCID 178491777, compound

https://huagongshe.com/reaction/1827259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycineHCID 750—
ReactantD-PhenylalanineHCID 71567—
ReactantN-Methyl-L-valineHCID 444080—
Reactant4-tert-Butyl hydrogen L-aspartateHCID 7010570—
ReactantTrifluoroacetic acid methylene chlorideHCID 21863450—
ReactantHCID 178491778HCID 178491778—
ReactantHCID 178491779HCID 178491779—
ProductHCID 178491777HCID 178491777—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053041B1
Source datasetuspto-grants-2006_05
ORD IDord-8a1f3e9205a64558bb261b5185b2c6ca
Source noteuspto-grants-2006_05