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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 48559Erstellt: 23. Oktober 2026

Dimethylformamide → (R)-9-[2-(N-Boc-L-valyloxymethyl)4-(stearoyloxy)butyl]guanine

https://huagongshe.com/de/reaction/48559

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktDicyclohexylcarbodiimideHCID 10868—
EduktBoc-L-ValineHCID 83693—
Edukt(R)-9-[2-Hydroxymethyl-4-(stearoyloxy)butyl]guanineHCID 136343267—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
Produkt(R)-9-[2-(N-Boc-L-valyloxymethyl)4-(stearoyloxy)butyl]guanineHCID 13582946039,3%

Reaktionsschritte

A mixture of N-Boc-L-valine (528 mg; 2.1 mmol) and N,N′-dicyclohexyl carbodiimide (250 mg; 1.21 mg) in dichloromethane (20 ml) was stirred over night at room temperature, dicyclohexylurea filtered off and extracted with a small volume of dichloromethane, and the filtrate evaporated in vacuo to a small volume. (R)-9-[2-Hydroxymethyl-4-(stearoyloxy)butyl]guanine (340 mg; 0.654 mmol), 4-dimethylaminopyridine (25 mg; 0.205 mmol), and dry N,N-dimethylformamide (15 ml) were added and the mixture was stirred for 4 h at 50° C. under N2. The solvent was evaporated in vacuo to a small volume. Column chromatography on silica gel, then on aluminum oxide (ethyl acetate:methanol: water 15:2:1 as eluent) gave 185 mg (39%) pure title compound as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06703394B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-fd5c64ed8b2a4ec8b5c23cabdd62366f
Quellennotizuspto-grants-2004_03