HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666201Generated: October 26, 2026
Potassium Carbonate → 9-(1-tert-Butoxycarbonylpiperidin-4-ylethyl)-8-methoxy-2-(2-methoxyethoxy)adenine
https://huagongshe.com/reaction/1666201
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl 4-(2-((methanesulfonyl)oxy)ethyl)piperidine-1-carboxylate | HCID 15229596 | — |
| Reactant | 8-Methoxy-2-(2-methoxyethoxy)-9H-purine-6-amine | HCID 57699791 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 9-(1-tert-Butoxycarbonylpiperidin-4-ylethyl)-8-methoxy-2-(2-methoxyethoxy)adenine | HCID 59288021 | 60% |
Reaction Steps
8-Methoxy-2-(2-methoxyethoxy)adenine (3.27 g, 13.7 mmol) was dissolved in DMF (75 ml), and thereto were added potassium carbonate (1.89 g, 13.7 mmol) and 4-[2-(methanesulfonyloxy)ethyl]piperidine-1-carboxylic acid tert-butyl ester (4.21 g, 13.7 mmol), and the mixture was stirred at 60° C. for 2.5 hours. The mixture was cooled to room temperature, and the carbonate salt was removed by filtration, and the filtrate was concentrated. To the residue was added water, and the mixture was extracted three times with chloroform. The resultant was dried over magnesium sulfate, and concentrated. The residue was purified by silica gel column (chloroform/methanol=200/1 to 100/1) to give the subtitle compound (3.62 g, 8.04 mmol) as a white solid. Yield: 60%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08044056B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-49af5b3e7cbe4db5a206163a0bd009bd |
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| Source note | uspto-grants-2011_10 |
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