Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 481486Erstellt: 26. Oktober 2026

Sodium Hydroxide → (2S,3S)-3-(5-(1-Cyanocyclopropyl)-2-methoxybenzyl)amino-2-phenylpiperidine

https://huagongshe.com/reaction/481486

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium HydroxideHCID 14798—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt5-(1-Cyanocyclopropyl)-2-methoxybenzaldehydeHCID 19066432—
Edukt(2S,3S)-2-Phenylpiperidin-3-amine dihydrochlorideHCID 69654807—
LösungsmittelDichloromethaneHCID 6344—
Produkt(2S,3S)-3-(5-(1-Cyanocyclopropyl)-2-methoxybenzyl)amino-2-phenylpiperidineHCID 979904241%

Reaktionsschritte

To a stirred suspension of Compound 3 (150 mg, 0.60 mmol) and Compound 2 (145 mg, 0.72 mmol) in dry CH2Cl2 (5 ml) was added NaBH(OAc)3 (358 mg, 1.68 mmol) portionwise at room temperature. The reaction mixture was stirred at room temperature for 6 h. The mixture was basified to pH10-11 with 10% NaOH aq. with ice-cooling. The organic layer was separated and the aqueous layer was extracted with CH2Cl2. The combined solution was washed with brine, dried (MgSO4) and concentrated in vacuo to give crude product. The crude product (300 mg) was purified by column chromatography on silica gel with CH2Cl2 -MeOH (20:1-10:1) to give Compound 4 (89 mg, 41%) as a yellow viscous oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05789423
Quelldatensatzuspto-grants-1998_08
ORD IDord-eb5d9595d0754a179895ec8f0191ad83
Quellennotizuspto-grants-1998_08