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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene) | HCID 96831 | — |
| Reactant | Sodium bicarbonate water | HCID 86585896 | — |
| Reactant | HCID 86761231 | HCID 86761231 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 86761230 | HCID 86761230 | 91.4% |
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
| 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-105fe91a4573439cbd9980ec3a7d8c43 |
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| Source note | uspto-grants-2010_12 |
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