ChemicalBook--->CAS DataBase List--->72587-18-9

72587-18-9

72587-18-9 Structure

72587-18-9 Structure
IdentificationBack Directory
[Name]

2-CHLORO-5-(TRIFLUOROMETHYL)-3-PYRIDINAMINE
[CAS]

72587-18-9
[Synonyms]

2-CHLORO-5-(TRIFLUOROMETHYL)-3-PYRIDIMINE
2-Chloro-5-(trifluoroMethyl)pyridin-3-aMine
2-CHLORO-5-(TRIFLUOROMETHYL)-3-PYRIDINAMINE
5-(TRIFLUOROMETHYL)-3-AMINO-2-CHLOROPYRIDINE
3-Amino-2-chloro-5-(trifluoromethyl)pyridine
[EINECS(EC#)]

200-589-5
[Molecular Formula]

C6H4ClF3N2
[MDL Number]

MFCD07375383
[MOL File]

72587-18-9.mol
[Molecular Weight]

196.56
Chemical PropertiesBack Directory
[Boiling point ]

256.8±40.0 °C(Predicted)
[density ]

1.507±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[form ]

Solid
[pka]

-0.29±0.10(Predicted)
[color ]

Off-white to brown
[Water Solubility ]

Slightly soluble in water.
[CAS DataBase Reference]

72587-18-9
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H312-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P304+P340-P305+P351+P338-P405-P501a
[HazardClass ]

IRRITANT
[HS Code ]

2933399990
Hazard InformationBack Directory
[Uses]

It's employed as a intermediate for pharmaceutical.
[Synthesis]

2-CHLORO-3-NITRO-5-(TRIFLUOROMETHYL)PYRIDINE

72587-15-6

2-CHLORO-5-(TRIFLUOROMETHYL)-3-PYRIDINAMINE

72587-18-9

The general procedure for the synthesis of 3-amino-2-chloro-5-(trifluoromethyl)pyridine from 5-(trifluoromethyl)-3-nitro-2-chloropyridine was as follows: zinc(II) dichloride dihydrate (4.39 g, 19.5 mmol) was added to 2-chloro-3-nitro-5-(trifluoromethyl)pyridine (1.00 g, 4.41 mmol) in ethyl acetate (25 mL) solution. The resulting suspension was stirred at 80°C for 2 hours. Upon completion of the reaction, the mixture was cooled to room temperature and then slowly added dropwise to an ice-cooled saturated sodium bicarbonate solution (100 mL). After the temperature was brought to room temperature, the product was separated. The suspension was filtered through a diatomaceous earth layer and the residue was washed four times with ethyl acetate (50 mL each time). The filtrate and washings were combined and washed sequentially with saturated sodium bicarbonate solution, water and saturated aqueous sodium chloride solution. The organic phase was dried over magnesium sulfate, filtered and concentrated to dryness. Yield: 0.78 g (90%). 1H-NMR (CD2Cl2, 400 MHz) data were as follows: δ=4.4 (br s, 2H), 7.24 (d, 1H), 8.02 (d, 1H).

[References]

[1] Patent: US2012/319050, 2012, A1. Location in patent: Page/Page column 64-65
[2] Patent: WO2012/172482, 2012, A1. Location in patent: Page/Page column 126
[3] Patent: WO2017/133657, 2017, A1. Location in patent: Page/Page column 64
[4] Patent: WO2017/133667, 2017, A1. Location in patent: Page/Page column 175; 176
Spectrum DetailBack Directory
[Spectrum Detail]

2-CHLORO-5-(TRIFLUOROMETHYL)-3-PYRIDINAMINE(72587-18-9)1HNMR
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