HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2-Aminopyrimidine-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloropyrimidine-4-carboxamide | HCID 247028 | — |
| Product | 2-Aminopyrimidine-4-carboxamide | HCID 18980287 | — |
Reaction Steps
The amine of formula (V) is thus obtained, and this is reacted with 2-chloropyrimidine-4-carboxamide of formula (VI) in an aprotic solvent, for example dimethylformamide, in the presence of a base, for example potassium carbonate, at a temperature of 20° to 80° C., especially 20° C. to 40° C., to give a 2-aminopyrimidine-4-carboxamide derivative of formula (I). The compound of formula (I) is, if desired, converted into an acid addition salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05164397 |
| Source dataset | uspto-grants-1992_11 |
| ORD ID | ord-750e7675d992434190c9565c5c2ec633 |
| Source note | uspto-grants-1992_11 |