HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acryloyl chloride → HCID 68388399, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | HCID 68388374 | HCID 68388374 | — |
| Reactant | HCID 68388482 | HCID 68388482 | — |
| Product | HCID 68388399 | HCID 68388399 | — |
Reaction Steps
As an example, N-(3-(6-((4-(4-methylpiperazin-1-yl)phenyl)amino)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)phenyl)acrylamide be prepared according to Route III. Beginning with 4-(3-aminophenyl)-N-(4-(4-methylpiperazin-1-yl)phenyl)-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-6-amine, acylation with acryloyl chloride provides N-(3-(6-((4-(4-methylpiperazin-1-yl)phenyl)amino)-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)phenyl)acrylamide. Deprotection under mild acidic conditions yields N-(3-(6-((4-(4-methylpiperazin-1-yl)phenyl)amino)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)phenyl)acrylamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09206176B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-482758995dc84d6da691e9169ad64bb5 |
| Source note | uspto-grants-2015_12 |