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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1396898Erstellt: 26. Oktober 2026

phenylmethyl (3S)-2-[(2R)-3-cyclopentyl-2-({formyl[(phenylmethyl)oxy]amino}methyl)propanoyl]-3-[(4-pyrimidinylamino)carbonyl]-1-pyrazolidinecarboxylate → (3S)-2-((2R)-3-cyclopentyl-2-{[formyl(hydroxy)amino]methyl}propanoyl)-N-4-pyrimidinyl-3-pyrazolidinecarboxamide

https://huagongshe.com/reaction/1396898

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktphenylmethyl (3S)-2-[(2R)-3-cyclopentyl-2-({formyl[(phenylmethyl)oxy]amino}methyl)propanoyl]-3-[(4-pyrimidinylamino)carbonyl]-1-pyrazolidinecarboxylateHCID 86706355—
KatalysatorPalladium hydroxideHCID 9942167—
LösungsmittelMethanolHCID 887—
Produkt(3S)-2-((2R)-3-cyclopentyl-2-{[formyl(hydroxy)amino]methyl}propanoyl)-N-4-pyrimidinyl-3-pyrazolidinecarboxamideHCID 6654843172,4%

Reaktionsschritte

A mixture of phenylmethyl (3S)-2-[(2R)-3-cyclopentyl-2-({formyl[(phenylmethyl)oxy]amino}methyl)propanoyl]-3-[(4-pyrimidinylamino)carbonyl]-1-pyrazolidinecarboxylate (1.21 g, 1.96 mmol) and Pearlman's catalyst (0.276 g, 0.39 mmol) in methanol (109 ml) was degassed and placed under 1 atm of H2 at 25° C. After 2 hrs, the reaction mixture was filtered and concentrated. Purification by reverse phase HPLC (Gilson) provided (3S)-2-((2R)-3-cyclopentyl-2-{[formyl(hydroxy)amino]methyl}propanoyl)-N-4-pyrimidinyl-3-pyrazolidinecarboxamide (554 mg, 70% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08901119B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-f67dea67b5254abf83ab7e4dbdd92063
Quellennotizuspto-grants-2014_12