Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromoacetamide | HCID 69632 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 86612504 | HCID 86612504 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86612503 | HCID 86612503 | 32.2% |
Reaction Steps
4-(4-Methoxy-3-trifluoromethyl-phenyl)-6-piperazin-1-yl-pyrimidine-2-carbonitrile trifluoroacetic acid salt (50 mg), diisopropylethylamine (40 mg) and 2-bromoacetamide (22 mg) were dissolved in acetonitrile (2 ml) and the mixture was stirred at 65° C. overnight. Mixture was partitioned between ethyl acetate (10 ml) and water (10 ml), organics were dried and evaporated under reduced pressure to afford a white solid. Purification by prep-HPLC afforded 18 mg of 2-{4-[2-Cyano-6-(4-methoxy-3-trifluoromethyl-phenyl)-pyrimidin-4-yl]-piperazin-1-yl}-acetamide trifluoroacetic acid salt as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07326715B2 |
|---|
| Source dataset | uspto-grants-2008_02 |
|---|
| ORD ID | ord-5dcaf168f66f438d86c8dffa8d517f8b |
|---|
| Source note | uspto-grants-2008_02 |
|---|