Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1489476Erstellt: 26. Oktober 2026

Triethylamine → (S)-N-[1-(amino-imino-methyl)-piperidin-3-ylmethyl]-benzamide (R)-hydroxy-phenylacetate

https://huagongshe.com/reaction/1489476

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktMethanesulfonic acid, aminoimino-HCID 9877361—
Edukt(R)-N-piperidin-3-ylmethyl-benzamide (R)-hydroxy-phenyl-acetateHCID 70050196—
LösungsmittelDimethylformamideHCID 6228—
Produkt(S)-N-[1-(amino-imino-methyl)-piperidin-3-ylmethyl]-benzamide (R)-hydroxy-phenylacetateHCID 8674861562,4%

Reaktionsschritte

Bc) 19.3 g of the mandelic acid salt obtained under Bb) are suspended in 193 ml of DMF, treated with 21.7 ml of triethylamine and 7.75 g of formamidinesulfonic acid and stirred at room temperature. The reaction mixture is evaporated and the residue is chromatographed on RP-18 silica gel with a water-acetonitrile gradient. There are isolated 13.4 g of (S)-N-[1-(amino-imino-methyl)-piperidin-3-ylmethyl]-benzamide (R)-hydroxy-phenyl-acetate (1:1), MS (FAB): 218 M-(H2N--CN).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05677448
Quelldatensatzuspto-grants-1997_10
ORD IDord-2c73f8d2c19a425893bff09943551c0a
Quellennotizuspto-grants-1997_10