Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(Bromomethyl)-1,1-difluorocyclopropane | HCID 2761402 | — |
| Reactant | HCID 44612737 | HCID 44612737 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58255013 | HCID 58255013 | — |
Reaction Steps
A mixture of N2-(2-fluoro-5-methyl-4-(piperidin-4-yl)phenyl)-N4-(5-methyl-1H-pyrazol-3-yl)-5-(trifluoromethyl)pyrimidine-2,4-diamine (100 mg, 0.22 mmol), 2-(bromomethyl)-1,1-difluorocyclopropane (76.4 mg, 0.45 mmol) and triethylamine (60.6 μL, 0.42 mmol) in 1 mL of DMF was heated at 60° C. in a microwave reactor for 2 h. The crude product was purified by RP-HPLC to afford N2-(4-(1-((2,2-difluorocyclopropyl)methyl)piperidin-4-yl)-2-fluoro-5-methylphenyl)-N4-(5-methyl-1H-pyrazol-3-yl)-5-(trifluoromethyl)pyrimidine-2,4-diamine; ESMS m/z 540.2 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08859574B2 |
|---|
| Source dataset | uspto-grants-2014_10 |
|---|
| ORD ID | ord-8e737eebd30545629b56620e8d5db8a8 |
|---|
| Source note | uspto-grants-2014_10 |
|---|