Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propylamine | HCID 7852 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 53410282 | HCID 53410282 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 53261243 | HCID 53261243 | 82% |
Reaction Steps
100 mg of 6-chloro-N-(4-methoxyphenyl)pyrimidine-4-amine in the form of a hydrochloride, 66 mg of propylamine and 120 mg of DIPEA were dissolved in 1 mL of n-BuOH and the mixture obtained was charged into a microwave vial and the vial obtained was heated to 200° C. for 60 minutes under microwave irradiation. Progress of the reaction was monitored by TLC. Upon termination of the reaction n-BuOH was evaporated off and the evaporation residue was subjected to crystallization from n-BuOH-EtOH solvent mixture. N4-(4-Methoxyphenyl)-N6-propylpyrimidine-4,6-diamine was obtained in the form of a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08986994B2 |
|---|
| Source dataset | uspto-grants-2015_03 |
|---|
| ORD ID | ord-459013835e17458f8ae9f87d82214ef3 |
|---|
| Source note | uspto-grants-2015_03 |
|---|
