HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrabutylammonium Fluoride → 8-(3-Pyridinyl)adenosine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 2',3',5'-Tris-o-(tert-butyldimethylsilyl)-8-(3-pyridinyl)adenosine | HCID 66906775 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-(3-Pyridinyl)adenosine | HCID 66906425 | — |
Reaction Steps
A solution of 2′,3′,5′-tris-O-(tert-butyldimethylsilyl)-8-(3-pyridinyl)adenosine (16c) (0.56 g, 0.82 mmol) and TBAF (0.85 g, 3.26 mmol) in THF (31 ml) under argon was stirred at room temperature overnight. The solvent was distilled off and the residual material dissolved in MeOH (10 ml). The solution was left at 0° C. overnight and the title compound isolated by filtration. 13C NMR: (75 MHz, DMSO); δ 62.27 (C-5′), 71.13/71.62 (C-2′, C-3′), 86.95/89.27 (C-4, C-1), 119.33/123.69/125.71/137.20/148.20/149.80/149.85/150.88/152.33/156.34 (C-5, C-5″, C-3″, C-4″, C-6, C-8, C-6″, C-2″, C-2, C-4). MS (EI): 344 (M, 2%), 255 (5), 241 (5), 213 (22), 212 (100), 211 (5) 185 (12), 104 (12).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08153609B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-2feb1e3ce04442feaeb3e05f54cb03dc |
| Source note | uspto-grants-2012_04 |