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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16706Erstellt: 23. Oktober 2026

Sodium Bicarbonate → HCID 178501220, Verbindung

https://huagongshe.com/de/reaction/16706

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium BicarbonateHCID 516892—
Edukttert-butyl N-(2-oxoethyl)carbamateHCID 4247255—
EduktSodium triacetoxyborohydrideHCID 5049666—
EduktHCID 178501210HCID 178501210—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTriethylamineHCID 8471—
ProduktHCID 178501220HCID 17850122042%

Reaktionsschritte

Methyl trans-4-aminocyclohexanecarboxylate hydrochloride (1.22 g) obtained in Reference Example 2(1) is suspended in dichloromethane (10 ml), and thereto is added triethylamine (1.76 ml) and the mixture is stirred for several minutes. After a solution of t-butyl (2-oxoethyl)carbamate (1.00 g) in dichloromethane (5 ml) and sodium triacetoxy borohydride (1.46 g) are added successively under ice-cooling, the reaction solution is warmed to the room temperature and stirred for 15 hours. Saturated aqueous sodium hydrogen carbonate solution is poured to the reaction solution, and the mixture is extracted with chloroform. The organic layer is dried over sodium sulfate and evaporated to remove the solvent under reduced pressure. A portion (1.71 g) of the resulting residue (2.33 g) is purified by silica gel column chromatography (eluent: chloroform/methanol=10/1) to give methyl trans-4-({2-[(t-butoxycarbonyl)amino]ethyl}amino)-cyclohexanecarboxylate (793 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737161B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-a64d572eb4e34ab18c9971e3e2d6b989
Quellennotizuspto-grants-2010_06