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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 10551Erstellt: 25. Oktober 2026

Sodium Bicarbonate → 4-(4-Chloro-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidine

https://huagongshe.com/reaction/10551

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium BicarbonateHCID 516892—
Edukttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
EduktSodium borohydrideHCID 4311764—
Edukt4-Chloroisoquinolin-5-amineHCID 21979937—
KatalysatorTitanium isopropoxideHCID 11026—
LösungsmittelMethanolHCID 887—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-(4-Chloro-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidineHCID 2197985021,8%

Reaktionsschritte

According to the method of Example 103, Step A, a mixture of Intermediate 90 (121 mg), tert-butyl 4-oxo-1-piperidinecarboxylate (274 mg), titanium tetraisopropoxide (0.41 ml) and dichloromethane (7 ml) was stirred at room temperature for 138 hours. The reaction mixture was added with sodium borohydride (114 mg) and methanol (1 ml) and stirred for 1.5 hours with ice cooling. The reaction mixture was added with saturated aqueous sodium hydrogencarbonate (10 ml) with ice cooling and extracted twice with ethyl acetate (15 ml for each time). The organic layer was dried over anhydrous sodium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=1:1) to obtain the title compound (53.5 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07094789B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-72438e154c334ea6b03363a7903a683d
Quellennotizuspto-grants-2006_08