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HRID 1921916Erstellt: 25. Oktober 2026

1,1'-Carbonyldiimidazole → (5-Benzyloxycarbonylamino-6-hydroxy-hexyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1921916

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
EduktN6-Boc-N2-Cbz-DL-lysineHCID 294900—
EduktSodium borohydrideHCID 4311764—
EduktHCID 178418361HCID 178418361—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(5-Benzyloxycarbonylamino-6-hydroxy-hexyl)-carbamic acid tert-butyl esterHCID 1449853391%

Reaktionsschritte

To a stirred solution of 2-benzyloxycarbonylamino-6-tert-butoxycarbonylamino-hexanoic acid (Cbz-Lys(Boc)-OH) (Chem-Impex International, 3.8 g, 10 mmol) in THF (25 mL) in a 100 mL round flask was added 1,1′-carbonyldiimidazole (CDI) (1.7 g, 10.5 mmol) at room temperature. After 20 minutes, the THF solution was transferred via a Teflon cannula (+=2 mm) to a stirred solution of sodium borohydride (0.75 g, 20 mmol) in water (10 mL) in a 1 L round flask immersed in a water bath at 5-10° C. The addition caused a strong evolution of hydrogen gas and the mixture was stirred for a couple of hours. The volatiles were then removed on a rotovap, and the residue was dissolved in ethyl acetate (150 mL). The ethyl acetate solution was extracted successively with cold 1 N HCl (2×50 mL), saturated sodium bicarbonate solution (2×50 mL), brine (100 mL), and was dried with anhydrous sodium sulfate. The dried ethyl acetate solution was then pass through a one inch flash pad of silica gel, and concentrated to provide a colorless solid (3.3 g, 91%), TLC Rf=0.24 (95:5:2 EtOAc:MeOH:H2O).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08173800B2
Quelldatensatzuspto-grants-2012_05
ORD IDord-8e25d61d83e849aca3d53f69bee9f403
Quellennotizuspto-grants-2012_05