HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Fmoc-Gly-OH → L-Phenylalanine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Fmoc-Gly-OH | HCID 93124 | — |
| Edukt | Fmoc-L-tryptophan | HCID 978343 | — |
| Edukt | (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-phenylpropanoic acid | HCID 978356 | — |
| Edukt | N-Fmoc-L-isoleucine | HCID 2724629 | — |
| Edukt | (2S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)hexanoic acid | HCID 7009636 | — |
| Edukt | 4-tert-Butyl N-((9H-Fluoren-9-ylmethoxy)carbonyl)-D-aspartate | HCID 7018816 | — |
| Produkt | L-Phenylalanine | HCID 6140 | — |
| Produkt | L-Tryptophan | HCID 6305 | — |
| Produkt | L-Isoleucine | HCID 6306 | — |
| Produkt | N-Methylphenylalanine | HCID 6951135 | — |
Reaktionsschritte
By following essentially the procedure of Table 2 and sequentially coupling Fmoc-MePhe-OH, Fmoc-DAsp(OtBu)-OH, Fmoc-Ile-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 Asp 0.96 (1), Gly 1.04 (1), Ile 0.96 (1), MePhe 1.07 (1), Ahx 0.98 (1), Trp 0.61 (1), NH3 0.89. MS (FAB): m/e 895 (M-H)-.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05502164 |
| Quelldatensatz | uspto-grants-1996_03 |
| ORD ID | ord-52bc2b38e78540d6a794024196a29814 |
| Quellennotiz | uspto-grants-1996_03 |