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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262398Generated: November 2, 2026

1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene) → HCID 86761228, compound

https://huagongshe.com/reaction/2262398

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene)HCID 96831—
ReactantSodium bicarbonate waterHCID 86585896—
ReactantHCID 86761229HCID 86761229—
SolventPyridineHCID 1049—
ProductHCID 86761228HCID 8676122876.4%

Reaction Steps

The above-obtained 2-N-carbamoyl-6-O-diphenylcarbamoyldeoxyguanosine (1.19 g, 2.35 mmol) was azeotroped with anhydrous pyridine three times and dissolved in anhydrous pyridine (23 mL), and 4,4′-dimethoxytrityl chloride (917 mg, 2.70 mmol) was added thereto. The mixture was stirred at room temperature for 2 hours, and sodium bicarbonate water (8 mL) was added thereto to terminate the reaction. Then, the reaction solution was extracted with ethyl acetate (150 mL)/sodium bicarbonate water (120 mL) once and then with ethyl acetate (150 mL)/brine (100 mL) twice. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (N60: spherical neutral silica gel) with methanol/2% to 3% chloroform containing 1% triethylamine to give 2-N-carbamoyl-5′-O-(4,4′-dimethoxytrityl)-6-O-diphenylcarbamoyldeoxyguanosine (1.45 g, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851157B1
Source datasetuspto-grants-2010_12
ORD IDord-38700cc77094462a9db8482f5189b534
Source noteuspto-grants-2010_12