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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1369334Erstellt: 25. Oktober 2026

N,N'-Dicyclohexylurea → (R)-9-[2(L-Valyloxymethyl)-4-(stearoyloxy)butyl]guanine

https://huagongshe.com/reaction/1369334

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,N'-DicyclohexylureaHCID 4277—
EduktDicyclohexylcarbodiimideHCID 10868—
EduktBoc-L-ValineHCID 83693—
Edukt(R)-9-[2-Hydroxymethyl-4-(stearoyloxy)butyl]guanineHCID 136343267—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
Produkt(R)-9-[2(L-Valyloxymethyl)-4-(stearoyloxy)butyl]guanineHCID 13542339545,7%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

A mixture of N-Boc-L-valine (528 mg; 2.1 mmol) and N,N′-dicyclohexyl carbodiimide (250 mg; 1.21 mmol) 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, their 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
PatentnummerUS06576763B1
Quelldatensatzuspto-grants-2003_06
ORD IDord-d3660a85af1547cabea23c4b4d64dff1
Quellennotizuspto-grants-2003_06