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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1441193Erstellt: 26. Oktober 2026

Fmoc-Gly-OH → L-Phenylalanine

https://huagongshe.com/reaction/1441193

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFmoc-Gly-OHHCID 93124—
EduktFmoc-L-tryptophanHCID 978343—
Edukt(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-phenylpropanoic acidHCID 978356—
Edukt(2S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)hexanoic acidHCID 7009636—
EduktN-alpha-(9-Fluorenylmethyloxycarbonyl)-N-alpha-methyl-L-aspartic acid beta-t-butyl esterHCID 7019716—
ProduktL-PhenylalanineHCID 6140—
ProduktL-TryptophanHCID 6305—
ProduktCaprineHCID 21236—
ProduktN-MethylphenylalanineHCID 6951135—

Reaktionsschritte

By following essentially the procedure of Table 2 and sequentially coupling Fmoc-MePhe-OH, Fmoc-MeAsp(OtBu)-OH, Fmoc-Ahx-OH, Fmoc-Trp-OH, Fmoc-Gly-OH, Fmoc-Ahx-OH and Hpa-OSu, the title compound was prepared. Amino Acid analysis following acid decomposition gave MeAsp 1.01 (1), Gly 1.05 (1), MePhe 0.91 (1), Ahx 2.02 (2), Trp 0.84 (1), NH3 0.82. MS (FAB): m/e 909 (M-H)-.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05502164
Quelldatensatzuspto-grants-1996_03
ORD IDord-0e70947c102c424092ae9d4f378d191a
Quellennotizuspto-grants-1996_03