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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1636791Erstellt: 26. Oktober 2026

Acetonitrile → 5-Pyridin-3-yl-thiophene-2-sulfonic acid [1-(2-amino-5-cyano-benzyl)-2-oxo-pyrrolidin-3-(S)-yl]-amide

https://huagongshe.com/reaction/1636791

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetonitrileHCID 6342—
Edukt5-Pyridin-3-yl-thiophene-2-sulfonyl chlorideHCID 10658976—
Edukt3-(3-(S)-Amino-2-oxopyrrolidin-1-ylmethyl)benzonitrile hydrochlorideHCID 22870786—
Produkt5-Pyridin-3-yl-thiophene-2-sulfonic acid [1-(2-amino-5-cyano-benzyl)-2-oxo-pyrrolidin-3-(S)-yl]-amideHCID 53688990—

Reaktionsschritte

The title compound is prepared in CH3CN instead of CH2Cl2 as described in EXAMPLE 1, Part E using 5-pyridin-3-yl-thiophene-2-sulfonyl chloride in place of benzo[b]thiophene-2-sulfonyl chloride and substituting 4-amino-[3-(3-(S)-amino-2-oxo-pyrrolidin-1-ylmethyl)]-benzonitrile dihydrochloride for 3-(3-(S)-amino-2-oxo-pyrrolidin-1-ylmethyl)-benzonitrile hydrochloride. The crude product is obtained by diluting with ethyl acetate and washing with saturated sodium bicarbonate (aq.), water and brine. The organic layer is dried over MgSO, filtered and concentrated. The crude product is purified by column chromatography eluting with 50% EtOAc/CH2Cl2 to give a light brown solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06034093
Quelldatensatzuspto-grants-2000_03
ORD IDord-ca3101b4b8954db28f32373cd6bb8de2
Quellennotizuspto-grants-2000_03