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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 223586Erstellt: 24. Oktober 2026

Neoviridogrisein IV → N-Methyl-N-phenyl-glycine

https://huagongshe.com/de/reaction/223586

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNeoviridogrisein IVHCID 196972—
Edukt3-Hydroxy-N-(24-Hydroxy-7,11,13,17,20-Pentamethyl-16-(3-Methylbutan-2-Yl)-3-(2-Methylpropyl)-2,5,9,12,15,18,21-Heptaoxo-10-Phenyl-8-Oxa-1,4,11,14,17,20-Hexazabicyclo(20.3.0)Pentacosan-6-Yl)Pyridine-2-CarboxamideHCID 417256—
Edukt(1S,9R,11S,12Z,14Z,19Z,22R)-9,11-Dihydroxy-22-methyl-6,23-dioxa-26-thia-2,17,27-triazatricyclo[17.5.2.14,7]heptacosa-4,7(27),12,14,19-pentaene-3,18,24-trioneHCID 6441064—
ProduktN-Methyl-N-phenyl-glycineHCID 420843—

Reaktionsschritte

In addition the identity of neoviridogrisein IV with viridogrisein was further confirmed by IR, UV, NMR and mass spectrometry, thin layer chromatography, hydrolysate analysis and antimicrobial spectrometry. On the other hand, the griseoviridin preparation obtained in Example 5 was crystallized in warm methanol to yield needle crystals. Then a part of the needle crystals were compared and identified with an authentic preparation of griseoviridin by IR, UV, NMR and mass spectrometry, thin layer chromatography, elementary analysis and other physico-chemical properties.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04355112
Quelldatensatzuspto-grants-1982_10
ORD IDord-517422c010fe47a2a29a2371a659c8a6
Quellennotizuspto-grants-1982_10