Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 12093257 | HCID 12093257 | — |
| Reactant | 2-amino-N-cyclopropyl-N-methylacetamide | HCID 12093258 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 9823773 | HCID 9823773 | 89% |
Reaction Steps
A mixture of 4-chloro-6-phenyl-2-(4-trifluoromethylphenyl)-pyrimidine (15 g), 2-amino-N-cyclopropyl-N-methylacetamide (10 g) and triethylamine (5.4 g) is heated at 150° C. under reflux for 2 hours. To the reaction mixture are added water and chloroform, and the chloroform layer is separated, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue is purified by silica gel column chromatography (eluent: chloroform), and recrystallized from ethanol to give the desired compound (17 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06620817B1 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-d813afdf16464cd98bb5579e47c813e4 |
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| Source note | uspto-grants-2003_09 |
|---|