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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene) | HCID 96831 | — |
| Reactant | Sodium bicarbonate water | HCID 86585896 | — |
| Reactant | HCID 86761229 | HCID 86761229 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 86761228 | HCID 86761228 | 76.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07851157B1 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-38700cc77094462a9db8482f5189b534 |
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| Source note | uspto-grants-2010_12 |
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