HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-Pyrazolo[3,4-d]pyrimidin-4-amine → HCID 178508725, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-Pyrazolo[3,4-d]pyrimidin-4-amine | HCID 75420 | — |
| Reactant | N-Iodosuccinamide | HCID 21864724 | — |
| Product | HCID 178508725 | HCID 178508725 | — |
Reaction Steps
Halogenation of commercially available 1H-pyrazolo[3,4-d]pyrimidin-4-amine provides an entry into the synthesis of compounds of Formula (I). In one embodiment, 1H-pyrazolo[3,4-d]pyrimidin-4-amine is treated with N-iodosuccinamide to give 3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine. Metal catalyzed cross coupling reactions are then carried out on 3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine. In one embodiment, palladium mediated cross-coupling of a suitably substituted phenyl boronic acid under basic conditions constructs intermediate A. Intermediate A is coupled via Mitsunobu reaction which undergoes further chemical modification to arrive at compound B.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08377946B1 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-e03fd868c7a24f21abd2f150bc7f8868 |
| Source note | uspto-grants-2013_02 |