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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 368715Erstellt: 23. Oktober 2026

1-Iodooctadecane → 2,6-Diamino-9-(2-O-octadecyl-beta-D-ribofuranosyl)purine

https://huagongshe.com/de/reaction/368715

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-IodooctadecaneHCID 12402—
EduktSodium hydrideHCID 24758—
Edukt2-AminoadenosineHCID 72200—
LösungsmittelDimethylformamideHCID 6228—
Produkt2,6-Diamino-9-(2-O-octadecyl-beta-D-ribofuranosyl)purineHCID 1173118711,4%

Reaktionsschritte

2,6-Diamino-9-(β-D-ribofuranosyl)purine (50 g, 180 mmol) and sodium hydride (7 g) in DMF (1 l) were heated to boiling for 2 hr. Iodooctadecane (100 g) was added at 150° C. and the reaction mixture allowed to cool to RT. The reaction mixture was stirred for 11 days at RT. The solvent was evaporated and the residue purified by silica gel chromatography. The product was eluted with 5% MeOH/CH2Cl2. The product containing fraction were evaporated to yield the product (11 g). 1H NMR (DMSO-d6) δ 0.84 (t, 3, CH2); 1.22 [m, 32, O--CH2 --CH2 --(CH2)16 --]; 1.86 (m, 2, O--CH2CH2 --); 3.25 (m, 2, O--CH2 --); 3.93 (d, 1, 4'H), 4.25 (m, 1, 3'H); 4.38 (t, 1, 2'H); 5.08 (d, 1, 3'-OH); 5.48 (t, 1, 5'-OH); 5.75 (s, 2, 6-NH2); 5.84 (d, 1, 1'-H); 6.8 (s, 2, 2-NH2); and 7.95 (s, 1, 8-H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06133438
Quelldatensatzuspto-grants-2000_10
ORD IDord-0bc1e61b368343588b8e2f9ae006fec7
Quellennotizuspto-grants-2000_10