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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 29080Erstellt: 25. Oktober 2026

1-Hydroxybenzotriazole → {(S)-2-[benzyloxylimino-methyl-pyrrolidine-1-yl]-1-cyclohexyl-2-oxo-ethyl}-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/29080

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-HydroxybenzotriazoleHCID 75771—
EduktDiisopropylethylamineHCID 81531—
EduktN-(tert-Butoxycarbonyl)-L-cyclohexylglycineHCID 7004938—
EduktPyrrolidine-2-carbaldehyde-O-benzyl-oximeHCID 72562396—
LösungsmittelDichloromethaneHCID 6344—
Produkt{(S)-2-[benzyloxylimino-methyl-pyrrolidine-1-yl]-1-cyclohexyl-2-oxo-ethyl}-carbamic acid tert-butyl esterHCID 86623471—

Reaktionsschritte

The solution of boc-L-α-cyclohexylglycine (1.27 g, 4.92 mmole), 1-hydroxylbenzotriazole (0.99 g, 7.38 mmole), diisopropylethylamine (2.54 g, 19.68 mmole), and O-benzotriazole-N,N,N,N-tetramethyl-urounium hexafluorophosphate (2.80 g, 7.38 mmole) in dichloromethane (30 ml) is stirred for 15 minutes at room temperature. A solution of pyrrolidine-2-carbaldehyde-O-benzyl-oxime (˜1.00 g, 0.49 mmole) in dichloromethane is added. The reaction solution is stirred for three hours at room temperature and then quenched with saturated NaHCO3 aqueous, extracted with dichloromethane. The organic layer is combined, dried, and concentrated under vacuum. The residue is purified by flash chromatography (silica gel; from 20% to 70% of ethyl acetate in hexane) to provide 1.81 g (83% over 2 steps) of the title compound. M+H+=444.2

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07419975B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-71d78ba436c044e7892fe799b4ab8c95
Quellennotizuspto-grants-2008_09