HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403899Generated: October 31, 2026
Dimethyl Sulfoxide → 6-Amino-2-(butyloxy)-9-{[1-(1-methylethyl)-3-piperidinyl]methyl}-7,9-dihydro-8H-purin-8-one
https://huagongshe.com/reaction/2403899
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-butoxy-8-methoxy 9-(piperidin-3-ylmethyl)-9H-purin-6-amine | HCID 58306241 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Amino-2-(butyloxy)-9-{[1-(1-methylethyl)-3-piperidinyl]methyl}-7,9-dihydro-8H-purin-8-one | HCID 67234538 | 30.6% |
Reaction Steps
2-Iodopropane (0.1 mmol) was weighed into a vial and an aliquot (0.3 ml, 0.1 mmol) of a solution of 2-(butyloxy)-8-(methyloxy)-9-(3-piperidinylmethyl)-9H-purin-6-amine (802 mg, 2.398 mmol) suspended in DMF (7.2 ml) was added. DIPEA (40 μl, 0.229 mmol) was added and the tube was capped and shaken to aid dispersion then allowed to stand at room temperature (18 hours). DMSO (400 uL) was added and the mixture purified by Mass Directed AutoPrep (Method A). The solvent was evaporated in vacuo using the Genevac. The residue was redissolved in 4M HCl/dioxane (0.5 ml), capped and stood at room temperature for 18 hours. The solvent was dried under a stream of nitrogen in the Radleys blowdown apparatus. The material was redissolved in methanol (0.5 ml), and applied to a 0.5 g aminopropyl SPE (preconditioned with methanol, 2 CV). The cartridge was eluted with methanol (2 ml), the solvent was removed to give the title compound (11.1 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802684B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-57eeacfea0f44cfeace7341a9338b4dc |
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| Source note | uspto-grants-2014_08 |
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