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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 643149Erstellt: 24. Oktober 2026

Triethylamine → methyl (S)-2-(4-amino-3-chloro-5-trifluoromethyl-benzyl)-4-[4-(6-hydroxy-2-oxo-1,4-dihydro-2H-quinazolin-3-yl)-piperidin-1-yl]-4-oxo-butanoate

https://huagongshe.com/de/reaction/643149

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktSodium BicarbonateHCID 516892—
EduktO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Edukt6-Hydroxy-3-piperidin-4-yl-3,4-dihydro-1H-quinazolin-2-oneHCID 21102207—
Edukt1-methyl (S)-2-(4-amino-3-chloro-5-trifluoromethyl-benzyl)-succinateHCID 86604295—
LösungsmittelDimethylformamideHCID 6228—
Produktmethyl (S)-2-(4-amino-3-chloro-5-trifluoromethyl-benzyl)-4-[4-(6-hydroxy-2-oxo-1,4-dihydro-2H-quinazolin-3-yl)-piperidin-1-yl]-4-oxo-butanoateHCID 69071695—

Reaktionsschritte

A solution of 1.37 g (4.04 mmol) 1-methyl (S)-2-(4-amino-3-chloro-5-trifluoromethyl-benzyl)-succinate, 1.42 g (4.40 mmol) TBTU, 0.63 mL (4.50 mmol) triethylamine and 1.00 g (4.04 mmol) 6-hydroxy-3-piperidin-4-yl-3,4-dihydro-1H-quinazolin-2-one in 10 mL DMF was stirred for 3 h at RT. The reaction mixture was poured onto 300 mL saturated NaHCO3 solution, the precipitated substance was suction filtered, washed with 50 mL water and dried at 60° C. in the circulating air dryer.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07696209B2
Quelldatensatzuspto-grants-2010_04
ORD IDord-42f657904f034372909ef82d7e496329
Quellennotizuspto-grants-2010_04