HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylcarbamoyl Chloride → N-(3-trifluoromethyl-phenyl)-4-(2-cyano-4-pyridyl)-2-pyrimidineamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylcarbamoyl Chloride | HCID 6598 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | 4-[2-[[3-(Trifluoromethyl)phenyl]amino]pyrimidin-4-yl]pyridine 1-oxide | HCID 10592652 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-(3-trifluoromethyl-phenyl)-4-(2-cyano-4-pyridyl)-2-pyrimidineamine | HCID 19711150 | — |
Reaction Steps
0.8 g (2.41 mmol) of N-(3-trifluoromethyl-phenyl)-4-(N-oxido4-pyridyl)-2-pyrimidineamine is suspended in 40 ml of acetonitrile. 0.834 ml (6.65 mmol) of tri-methylsilyl cyanide and 0.611 ml (6.665 mmol) of dimethylcarbamoyl chloride are added and the reaction mixture is stirred for 12 hours at 60°. After concentration under reduced pressure, crystallisation is effected from tetrahydrofuran/diethyl ether. N-(3-trifluoromethyl-phenyl)-4-(2-cyano-4-pyridyl)-2-pyrimidineamine is obtained; m.p. 164°-166°, Rf =0.40 (n-hexane:ethyl acetate=1:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05705502 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-43ed1896744740fbbcd551bcc51b7f8e |
| Source note | uspto-grants-1998_01 |