HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447690Generated: October 29, 2026
Dimethylformamide → HCID 178425937, compound
https://huagongshe.com/reaction/447690
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 3-Thiocresol | HCID 7930 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-{[(1R,3S,4S)-3-{[tert-butyl(dimethyl)silyl]oxy}-4-({[tert-butyl(dimethyl)silyl]-oxy}methyl)cyclopentyl]oxy}-8-iodo-9-(tetrahydro-2H-pyran-2-yl)-9H-purine | HCID 66797940 | — |
| Product | HCID 178425937 | HCID 178425937 | 82.1% |
Reaction Steps
To a solution of 3-methylbenzenethiol (0.55 mL, 0.0046 mol) in DMF (10 mL, 0.2 mol) was added sodium hydride (0.093 g, 0.0023 mol). The mixture was stirred at room temperature for 10 minutes and then 6-{[(1R,3S,4S)-3-{[tert-butyl(dimethyl)silyl]oxy}-4-({[tert-butyl(dimethyl)silyl]oxy}methyl)cyclopentyl]oxy}-8-iodo-9-(tetrahydro-2H-pyran-2-yl)-9H-purine (400 mg, 0.0006 mol) (Example 115, steps a-b) was added and the solution was heated at 150° C. for 8 hours. The reaction was cooled, quenched by addition of water and the mixture was extracted with ethyl acetate, washed with water, brine, dried (Na2SO4), filtered and concentrated. The residue was purified by flash chromatography (0 to 30% ethyl acetate/hexanes) to obtain 296 mg (80%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481550B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-8029dc66c5e04572a854d89a671f3982 |
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| Source note | uspto-grants-2013_07 |
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