HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminophenol → 6-(cyclopentylamino)-N-(4-hydroxyphenyl)pyrimidine-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminophenol | HCID 403 | — |
| Reactant | 6-(Cyclopentylamino)pyrimidine-4-carboxylic acid | HCID 59447055 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 6-(cyclopentylamino)-N-(4-hydroxyphenyl)pyrimidine-4-carboxamide | HCID 25182623 | — |
Reaction Steps
Following the general method as outlined in Example 1, starting from 6-[(cyclopentyl)amino]pyrimidine-4-carboxylic acid (Intermediate 5) and 4-aminophenol (Aldrich), the title compound was obtained as a yellow solid after trituration in acetonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08399448B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-eaaeb7fa30d441efb8faf1b9d17cebb4 |
| Source note | uspto-grants-2013_03 |