Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 2-Iodoadenosine | HCID 169662 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | Sodium Acetate | HCID 517045 | — |
| Product | HCID 86592810 | HCID 86592810 | — |
Reaction Steps
2-Iodoadenosine (1, 2.93 g, 7.45 mmol) was dissolved in NaOAc buffer (1.0 M, pH 4, 50 ml) at 50° C. The solution was cooled to room temperature and bromine (0.46 mL, 8.94 mmol) was added. After stirring overnight at room temperature, adding NaHSO3 destroyed the excess of bromine and the pH of the solution was adjusted to 7 with NaOH solution (5 M). The reaction mixture was kept at 4° C. for 5 hr and the precipitate was filtered. The white solid was washed with water and dried. Yield 2.43 mg (5.14 mmol, 69%), Rƒ 0.69 (10% MeOH in EtOAc); 1H NMR (DMSO-d6) δ 7.91 (s, 2H, NH2), 5.77 (d, 1H, J=6.52 Hz, H-1′), 5.47 (d, 1H, J=5.84 Hz, OH-2′), 5.24 (d, 1H, J=4.80 Hz, OH-5′), 5.03–4.84 (m, 2H, OH-3′, H-2′), 4.20–4.09 (m, 1H, H-3′), 3.97–3.88 (m, 1H, H-4′), 3.71–3.42 (m, 2H, H-5′) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07112574B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-e7fba826e0b44033827d2c41683af3ae |
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| Source note | uspto-grants-2006_09 |
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