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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 913069Erstellt: 25. Oktober 2026

Acetic Acid → N-{3-[1-(4-Chloro-3-ethoxy-benzyl)-piperidin-4-ylamino]-phenyl}-acetamide

https://huagongshe.com/reaction/913069

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktTriethylamineHCID 8471—
EduktSodium cyanoborohydrideHCID 5003444—
Edukt4-Chloro-3-ethoxybenzaldehydeHCID 54775642—
EduktN-[3-(Piperidin-4-ylamino)-phenyl]-acetamide dihydrochlorideHCID 67400427—
LösungsmittelEthanolHCID 702—
ProduktN-{3-[1-(4-Chloro-3-ethoxy-benzyl)-piperidin-4-ylamino]-phenyl}-acetamideHCID 2485496812,4%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

To a solution of N-[3-(piperidin-4-ylamino)-phenyl]-acetamide dihydrochloride (61.2 mg, 0.2 mmol, 1.0 equiv; intermediate B1), acetic acid (60.1 mg, 1.0 mmol, 5.0 equiv) and triethylamine (40.5 mg, 0.4 mmol, 2.0 equiv) in ethanol (1 mL) was added 4-chloro-3-ethoxy-benzaldehyde (46.1 mg, 0.25 mmol, 1.25 equiv; intermediate E2, vide infra) and the mixture stirred at 50° C. After 1 h, sodium cyanoborohydride (15.1 mg, 0.24 mmol, 1.2 equiv), dissolved in ethanol (1 mL), was added and the mixture stirred at 50° C. over night. Removal of the solvent under reduced pressure and purification by preparative HPLC on reversed phase eluting with a gradient of acetonitrile/water provided 10.0 mg (12%) of the title compound. MS (ISP): 402.3 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08026255B2
Quelldatensatzuspto-grants-2011_09
ORD IDord-19cd267097e24998868990e89a31b09b
Quellennotizuspto-grants-2011_09