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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1827259생성일: 2026년 10월 25일

Glycine → HCID 178491777, 화합물

https://huagongshe.com/reaction/1827259

반응식

참여 물질

역할이름HCID투입량
반응물GlycineHCID 750—
반응물D-PhenylalanineHCID 71567—
반응물N-Methyl-L-valineHCID 444080—
반응물4-tert-Butyl hydrogen L-aspartateHCID 7010570—
반응물Trifluoroacetic acid methylene chlorideHCID 21863450—
반응물HCID 178491778HCID 178491778—
반응물HCID 178491779HCID 178491779—
생성물HCID 178491777HCID 178491777—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07053041B1
출처 데이터셋uspto-grants-2006_05
ORD IDord-8a1f3e9205a64558bb261b5185b2c6ca
출처 메모uspto-grants-2006_05