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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1694679Erstellt: 25. Oktober 2026

Pyridine → N2-phenoxyacetyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-(2-cyanoethoxymethyl)guanosine

https://huagongshe.com/reaction/1694679

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
Edukt1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene)HCID 96831—
EduktN2-Phenoxyacetyl-2'-O-(2-cyanoethoxymethyl)guanosineHCID 136387250—
LösungsmittelMethanolHCID 887—
ProduktN2-phenoxyacetyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-(2-cyanoethoxymethyl)guanosineHCID 13636840575,5%

Reaktionsschritte

N2-Phenoxyacetyl-2′-O-(2-cyanoethoxymethyl)guanosine (660 mg, 1.32 mmol) was subjected to azeotropic distillation with pyridine, and then was dried with a vacuum pump for 30 minutes. The residue was dissolved in 9 mL of THF, and 2.1 g of pyridine (26.4 mmol) and 600 mg of molecular sieve 4 A were added under an argon atmosphere, and the reaction solution was stirred for 10 minutes. To the solution was added 540 mg of 4,4′-dimethoxytritylchloride (1.58 mmol) by 3 portions every 1 hour, and the reaction solution was further stirred for 1 hour. After 2 mL of methanol was added and the reaction solution was stirred for 2 minutes, the reaction solution was filtrated with a celite, and was washed with ethyl acetate. After concentrating the filtrate with evaporation, the residue was dissolved in ethyl acetate, and was separated with a saturated aqueous sodium bicarbonate solution. After the organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, the solvent was distilled off. The obtained residue was purified by silica gel chromatography to obtain the objective compound (800 mg, yield 75%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08158775B2
Quelldatensatzuspto-grants-2012_04
ORD IDord-3b8c171a64114e159826fe15cd99a0e8
Quellennotizuspto-grants-2012_04