Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662292Generated: October 28, 2026

1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene) → 7-(2-Thienyl)-3-[5-O-(4,4'-dimethoxytrityl)-beta-D-ribofuranosyl]-3H-imidazo[4,5-b]pyridine

https://huagongshe.com/reaction/1662292

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene)HCID 96831—
ReactantSodium BicarbonateHCID 516892—
Reactant7-(2-Thienyl)-3-(beta-D-ribofuranosyl)-3H-imidazo[4,5-b]pyridineHCID 44433304—
SolventPyridineHCID 1049—
Product7-(2-Thienyl)-3-[5-O-(4,4'-dimethoxytrityl)-beta-D-ribofuranosyl]-3H-imidazo[4,5-b]pyridineHCID 6742980871.1%

Reaction Steps

Compound 11 (99 mg, 0.29 mmol) was azeotroped three times with anhydrous pyridine and then dissolved in pyridine (3.0 ml). To this solution, 4,4′-dimethoxytrityl chloride (106 mg, 0.31 mmol) was added, and the resulting mixture was stirred at room temperature for 2 hours. The reaction mixture was poured into 5% aqueous NaHCO3 and then extracted with ethyl acetate. The organic layer was washed three times with saturated aqueous sodium chloride, dried over Na2SO4, and then evaporated under reduced pressure to remove the solvent. The product was purified by silica gel column chromatography (1% methanol-CH2Cl2) to give Compound 12 (131 mg, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030478B2
Source datasetuspto-grants-2011_10
ORD IDord-d19a217e87d04e6ab55ce9ef14ec2a6c
Source noteuspto-grants-2011_10