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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262402Generated: October 31, 2026

1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene) → HCID 86761230, compound

https://huagongshe.com/reaction/2262402

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene)HCID 96831—
ReactantSodium bicarbonate waterHCID 86585896—
ReactantHCID 86761231HCID 86761231—
SolventPyridineHCID 1049—
ProductHCID 86761230HCID 8676123091.4%

Reaction Steps

The above-obtained 6-O-diphenylcarbamoyl-2-N-methylthiocarbamoyldeoxyguanosine (400 mg, 0.744 mmol) was azeotroped with anhydrous pyridine three times and dissolved in anhydrous pyridine (8.0 mL), and 4,4′-dimethoxytrityl chloride (278 mg, 0.818 mmol) was added thereto. The mixture was stirred at room temperature for 3 hours, and then sodium bicarbonate water (3 mL) was added thereto to terminate the reaction. The reaction solution was extracted with ethyl acetate (150 mL)/sodium bicarbonate water (120 mL) once and with ethyl acetate (150 mL)/brine (100 mL) twice. Then, the organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (N60: spherical neutral silica gel) with methanol/3% to 4% chloroform containing 1% triethylamine to give 5′-O-(4,4′-dimethoxytrityl)-6-O-diphenylcarbamoyl-2-N-methylthiocarbamoyldeoxyguanosine (570 mg, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851157B1
Source datasetuspto-grants-2010_12
ORD IDord-105fe91a4573439cbd9980ec3a7d8c43
Source noteuspto-grants-2010_12