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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792093Generated: November 4, 2026

1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene) → HCID 23397587, compound

https://huagongshe.com/reaction/1792093

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene)HCID 96831—
ReactantSodium BicarbonateHCID 516892—
ReactantN-(9-((2R,4S,5R)-5-((Tert-butyldimethylsilyloxy)methyl)-4-hydroxytetrahydrofuran-2-YL)-9H-purin-6-YL)benzamideHCID 13833804—
SolventPyridineHCID 1049—
ProductHCID 23397587HCID 2339758763.1%

Reaction Conditions

Temperature45 °C

Reaction Steps

N6-benzoyl-5′-O-(tert-butyldimethylsilyl)-2′-deoxyadenosine (16.1 g) was dissolved in 100 ml of anhydrous pyridine. 4,4′-dimethoxytrityl chloride (12.8 g) and anhydrous pyridine (140 ml) were further added, follow by stirring at 45° C. After the reaction completed, the reaction mixture was neutralized by sodium hydrogen carbonate, and pyridine was distilled off. Extraction using chloroform was carried out and the extract was washed by a saturated aqueous solution of sodium chloride and dried with anhydrous magnesium sulfate. The extract was concentrated and then purified by column chromatography (ethyl acetate/hexane) to obtain 16.7 g of the titled compound (yield: 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074917B2
Source datasetuspto-grants-2006_07
ORD IDord-18c7ff5220a5423189fd868f41a6727a
Source noteuspto-grants-2006_07