HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminoquinoline → 6-(cyclohexylamino)-N-quinolin-4-ylpyrimidine-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminoquinoline | HCID 68476 | — |
| Reactant | 6-(Cyclohexylamino)pyrimidine-4-carboxylic acid | HCID 59447075 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-(cyclohexylamino)-N-quinolin-4-ylpyrimidine-4-carboxamide | HCID 25182754 | — |
Reaction Steps
Following the general method as outlined in Example 1, starting from 6-(cyclohexylamino)pyrimidine-4-carboxylic acid (Intermediate 4) and 4-aminoquinoline (Tyger), the title compound was obtained as a red solid after trituration in methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09150519B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-217ccfb93fd646198155f8c06d0e1be1 |
| Source note | uspto-grants-2015_10 |