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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 420113Erstellt: 27. Oktober 2026

Imidazole → N-benzyl-O-methyl-N2-trityl-D-serinamide

https://huagongshe.com/reaction/420113

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazoleHCID 795—
EduktMethyl iodideHCID 6328—
EduktSodium hydrideHCID 24758—
EduktN-benzyl-N2-trityl-D-serinamideHCID 57734155—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-benzyl-O-methyl-N2-trityl-D-serinamideHCID 54752467—

Reaktionsbedingungen

Temperatur-15 °C

Reaktionsschritte

To a mixture of sodium hydride (6.59 g), imidazole (1.564 g) and tetrahydrofuran (150 ml), a solution of Example 5 product (i.e. N-benzyl-N2-trityl-D-serinamide, 50 g) in tetrahydrofuran (500 ml) was slowly added at −15° C. and the mixture was stirred for 45 minutes at −15° C. Methyl iodide (24.38 g) was slowly added to the mixture for 15 minutes at −15° C. to −5° C. and the formed reaction mixture was stirred at −5° C. for 3 hours. The reaction mixture was cooled to 0° C., water was added to it and then the tetrahydrofuran was recovered completely under vacuum at 40° C. Hexane (250 ml) was added to it and stirred for 15 minutes. The layers were separated and the aqueous layer was neutralized with acetic acid till pH=6.0. Dichloromethane (2×150 ml) was added to the aqueous layer and layers were separated. Oily product was recovered under vacuum at 35-40° C. from the organic layer. Hexane (100 ml) was added to the oily product and the solution formed is stirred for 15 minutes, filtered and dried to get the titled product of Formula Va.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08093426B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-22910e7ac9cd4e8795a8bbbbea8a3757
Quellennotizuspto-grants-2012_01