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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1943026Erstellt: 25. Oktober 2026

Acetic Acid → Tert-butyl 4-(2-{[(1-methyl-2-oxo-1,2-dihydroquinolin-3-yl)methyl]amino}-1-phenylethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1943026

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt1-Methyl-2-oxo-1,2-dihydroquinoline-3-carbaldehydeHCID 4914628—
EduktSodium triacetoxyborohydrideHCID 5049666—
EduktTert-butyl 4-(2-amino-1-phenylethyl)piperidine-1-carboxylateHCID 58415947—
LösungsmittelDichloromethaneHCID 6344—
ProduktTert-butyl 4-(2-{[(1-methyl-2-oxo-1,2-dihydroquinolin-3-yl)methyl]amino}-1-phenylethyl)piperidine-1-carboxylateHCID 58415941—

Reaktionsschritte

1-methyl-2-oxo-1,2-dihydroquinoline-3-carbaldehyde (0.590 g, 3.15 mmol), tert-butyl 4-(2-amino-1-phenylethyl)piperidine-1-carboxylate (1.2 g crude, 3.94 mmol), and acetic acid (0.677 ml, 11.83 mmol) were combined in CH2Cl2 (20 ml). Sodium triacetoxyborohydride (2.506 g, 11.83 mmol) was added and the reaction stirred for 16 hours. The mixture was partitioned between CH2Cl2 and satd. bicarb, the aqueous portion extracted 3×CH2Cl2, and the organic portion dried (Na2SO4) then concentrated in vacuo. The product was carried on without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08389720B2
Quelldatensatzuspto-grants-2013_03
ORD IDord-0353f2fd653b48548302c70aa6a7fef7
Quellennotizuspto-grants-2013_03