Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine chloride | HCID 24640 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Sodium Pyrosulfite | HCID 656671 | — |
| Reactant | 4-Methoxy-1H-pyrazolo[3,4-d]pyrimidin-6-amine | HCID 11252197 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178494242 | HCID 178494242 | — |
Reaction Steps
4-Methoxy-pyrazolo[3,4-d]pyrimidin-6-ylamine (6.75 g, 40.87 mmol) was suspended in an aqueous solution containing sodium acetate (6.0 g, 44.09 mmol) and iodine monochloride (9.12 g, 56.17 mmol) and stirred at 100° C. in a sealed reaction vessel for 24 h. The resulting mixture was cooled to room temperature and treated with a solution of sodium metabisulfite (3.6 g, 18.94 mmol) in 24 mL of water. The solid that formed was filtered, rinsed with water and dried: 6.93 g (58%) yield; TLC (10% methanol in ethyl acetate), Rf=0.57; 1H NMR (DMSO-d6) δ 13.08 (1H, br s, N−1 proton), 10.58 (1H, s, N−5 proton), 6.60 (2H, br s, 6-amino).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07751982B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-238c28f491b04880b37149646a271fe8 |
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| Source note | uspto-grants-2010_07 |
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