Identification | Back Directory | [Name]
5-Chloro-3-(trifluoromethyl)-2-pyridinamine | [CAS]
79456-33-0 | [Synonyms]
5-Chloro-3-(trifluoromethyl)-2-pyridinamine 5-Chloro-3-(trifluoroMethyl)pyridin-2-aMine 5-Chloro-3-trifluoroMethyl-pyridin-2-ylaMine 2-Pyridinamine, 5-chloro-3-(trifluoromethyl)- | [EINECS(EC#)]
200-258-5 | [Molecular Formula]
C6H4ClF3N2 | [MDL Number]
MFCD13185329 | [MOL File]
79456-33-0.mol | [Molecular Weight]
196.56 |
Chemical Properties | Back Directory | [Boiling point ]
218℃ | [density ]
1.507 | [Fp ]
85℃ | [storage temp. ]
under inert gas (nitrogen or Argon) at 2–8 °C | [pka]
1.95±0.49(Predicted) | [Appearance]
Off-white to light yellow Solid |
Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of 5-chloro-3-(trifluoromethyl)pyridin-2-amines from 2-amino-3-trifluoromethylpyridine:
Step A Synthesis of 5-chloro-3-(trifluoromethyl)-2-pyridinamine
[0120] To a solution of N,N-dimethylformamide (100 mL) containing 3-(trifluoromethyl)-2-pyridinamine (12.2 g, 75 mmol), N-chlorosuccinimide (10.5 g, 79 mmol) was added. The reaction mixture was heated to 60 °C and stirred continuously for 1 hour. Upon completion of the reaction, the mixture was cooled to room temperature and subsequently concentrated. The residue was purified by silica gel column chromatography using dichloromethane as eluent to give 5-chloro-3-(trifluoromethyl)pyridin-2-amine (13.0 g, 88% yield). m/z 197 (M + 1) by LCMS. | [References]
[1] Patent: WO2010/91411, 2010, A1. Location in patent: Page/Page column 88-89 [2] Patent: WO2011/41713, 2011, A2. Location in patent: Page/Page column 206 [3] Patent: WO2015/79224, 2015, A1. Location in patent: Page/Page column 60; 61 |
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