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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 446539Erstellt: 24. Oktober 2026

Sodium Bicarbonate → tert-Butyl 3-({6-[(2-{4-[(biphenyl-2-ylcarbamoyl)oxy]piperidin-1-yl}ethyl)(methyl)amino]-6-oxohexyl}amino)benzoate

https://huagongshe.com/de/reaction/446539

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium BicarbonateHCID 516892—
Edukttert-Butyl-3-aminobenzoateHCID 2737408—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt1-{2-[Methyl(6-oxohexanoyl)amino]ethyl}piperidin-4-yl biphenyl-2-ylcarbamateHCID 86761901—
LösungsmittelEthanolHCID 702—
LösungsmittelEthyl AcetateHCID 8857—
Produkttert-Butyl 3-({6-[(2-{4-[(biphenyl-2-ylcarbamoyl)oxy]piperidin-1-yl}ethyl)(methyl)amino]-6-oxohexyl}amino)benzoateHCID 8666344558%

Reaktionsschritte

The compound (100 mg, 0.215 mmol) obtained in Example 4g was dissolved in ethanol (6 mL), tert-butyl 3-aminobenzoate (54 mg, 0.279 mmol) and sodium triacetoxyborohydride (59 mg, 0.279 mmol) were added under ice cooling, and the mixture was stirred at room temperature under a nitrogen atmosphere for 16 hours. After the reaction was completed, a saturated aqueous sodium hydrogencarbonate solution was added, and ethyl acetate was further added to separate the layers. The organic layer was separated, washed with saturated sodium chloride solution, and then dried with anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the resulting residue was purified by NH silica gel column chromatography (ethyl acetate:methanol, 10:1, v/v) to give the title compound (80.0 mg; yield, 58%) as a colorless oily substance.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08476253B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-b8c89ba72486497f99469ffefc9bf37e
Quellennotizuspto-grants-2013_07