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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 10553Erstellt: 25. Oktober 2026

Sodium Bicarbonate → N-(tert-butoxycarbonyl)-N'-(4-chloro-5-isoquinolyl)-1,4-cyclohexanediamine

https://huagongshe.com/reaction/10553

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium BicarbonateHCID 516892—
EduktSodium borohydrideHCID 4311764—
Edukt4-Chloroisoquinolin-5-amineHCID 21979937—
EduktTert-butyl 4-oxo-1-aminocyclohexylcarboxylateHCID 21979990—
KatalysatorTitanium isopropoxideHCID 11026—
LösungsmittelMethanolHCID 887—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(tert-butoxycarbonyl)-N'-(4-chloro-5-isoquinolyl)-1,4-cyclohexanediamineHCID 21979991—

Reaktionsschritte

According to the method of Example 103, Step A, a mixture of Intermediate 90 (100 mg), tert-butyl 4-oxo-1-aminocyclohexylcarboxylate (270 mg), titanium tetraisopropoxide (0.34 ml) and dichloromethane (7 ml) was stirred at room temperature for 120 hours. The reaction mixture was added with sodium borohydride (94 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 then 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 (40.4 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07094789B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-2183330ad69d4daf8b0bf3debc9cee84
Quellennotizuspto-grants-2006_08