HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-Indazol-5-amine → 6-(cyclohexylamino)-N-1H-indazol-5-ylpyrimidine-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-Indazol-5-amine | HCID 88012 | — |
| Reactant | 6-(Cyclohexylamino)pyrimidine-4-carboxylic acid | HCID 59447075 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-(cyclohexylamino)-N-1H-indazol-5-ylpyrimidine-4-carboxamide | HCID 25182765 | — |
Reaction Steps
Following the general method as outlined in Example 1, starting from 6-(cyclohexylamino)pyrimidine-4-carboxylic acid (Intermediate 4) and 5-aminoindazole (Aldrich), the title compound was obtained as a pink solid after trituration in DCM.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09150519B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-f4e94e93c53340e6893ecfe45d35cd53 |
| Source note | uspto-grants-2015_10 |