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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1990796Erstellt: 25. Oktober 2026

Acetic Acid → Benzothiazol-2-yl-[1-(2-ethoxy-naphthalen-1-ylmethyl)-piperidin-4-yl]-amine

https://huagongshe.com/reaction/1990796

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktDiisopropylethylamineHCID 81531—
Edukt2-Ethoxynaphthalene-1-carbaldehydeHCID 88099—
EduktSodium cyanoborohydrideHCID 5003444—
EduktN-(Piperidin-4-yl)-1,3-benzothiazol-2-amineHCID 14575274—
LösungsmittelEthanolHCID 702—
ProduktBenzothiazol-2-yl-[1-(2-ethoxy-naphthalen-1-ylmethyl)-piperidin-4-yl]-amineHCID 866076258%

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

To a solution of benzothiazol-2-yl-piperidin-4-yl-amine (23.3 mg, 0.1 mmol, 1.0 equiv) and 2-ethoxy-naphthalene-1-carbaldehyde (commercially available, 24.0 mg, 0.12 mmol, 1.2 equiv) in ethanol (2 mL) was added diisopropylethylamine (23.42 μL, 25.9 mg, 0.2 mmol, 2.0 equiv) and acetic acid (18.0 mg, 0.3 mmol, 3.0 equiv) and the mixture stirred at 40° C. After 1 h, sodium cyano borohydride (7.54 mg, 0.12 mmol, 1.2 equiv) was added and the mixture stirred at 40° 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 3.3 mg (8%) of the title compound. MS (ESI): 418.4 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07645753B2
Quelldatensatzuspto-grants-2010_01
ORD IDord-8ee5054967184bad9481d5be680ac808
Quellennotizuspto-grants-2010_01