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HRID 1827259作成日:2026年10月27日

Glycine → HCID 178491777、化合物

https://huagongshe.com/reaction/1827259

反応式

関与物質

役割名称HCID仕込み量
反応物GlycineHCID 750—
反応物D-PhenylalanineHCID 71567—
反応物N-Methyl-L-valineHCID 444080—
反応物4-tert-Butyl hydrogen L-aspartateHCID 7010570—
反応物Trifluoroacetic acid methylene chlorideHCID 21863450—
反応物HCID 178491778HCID 178491778—
反応物HCID 178491779HCID 178491779—
生成物HCID 178491777HCID 178491777—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07053041B1
出典データセットuspto-grants-2006_05
ORD IDord-8a1f3e9205a64558bb261b5185b2c6ca
出典メモuspto-grants-2006_05