Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1H-Pyrazolo[3,4-d]pyrimidin-4-amine | HCID 75420 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178508725 | HCID 178508725 | 97% |
Reaction Steps
A mixture of 4-aminopyrazolo[3,4-d]pyrimidine (Intermediate KA) (11.75 g, 0.087 mol) and N-iodosuccinimide (25.45 g, 0.113 mol) in dimethylformamide (300 mL) was heated at 50° C. for 24 h. Additional N-iodosuccinimide (3.92 g, 0.017 mol) was added and heating at 50° C. was continued for another 24 h. The mixture was allowed to cool to ambient temperature and the volume was reduced by ⅓ under reduced pressure. Water (500 mL) was added to the resulting slurry to yield a dark brown precipitate which was collected by filtration, washed with water and ethanol and dried in vacuo to give 3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-ylamine as a light yellow powder (97%, 22 g, 0.084 mol): 1H NMR (DMSO-d6, 400 MHz) 13.81 (s, 1H), 8.17 (s, 1H), 2.73 (s, 1H), 2.57 (s, 1H); TLC (dichloromethane/methanol=9:1) Rf 0.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06921763B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-5022160d02bb427694ba5065fc663863 |
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| Source note | uspto-grants-2005_07 |
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