ChemicalBook--->CAS DataBase List--->317318-97-1

317318-97-1

317318-97-1 Structure

317318-97-1 Structure
IdentificationBack Directory
[Name]

Thiazole,5-(chloromethyl)-4-methyl-2-[4-(trifluoromethyl)phenyl]-
[CAS]

317318-97-1
[Synonyms]

ChloroMethylthiazole
5-Chloromethyl-4-methyl-2-(4-trifluoromethylphenyl)thiazole
4-[5-(Chloromethyl)-4-methyl-1,3-thiazol-2-yl]benzotrifluoride
5-(Chloromethyl)-4-methyl-2-[4-(trifluoromethyl)phenyl]-1,3-...
Thiazole,5-(chloromethyl)-4-methyl-2-[4-(trifluoromethyl)phenyl]-
5-(Chloromethyl)-4-methyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazole
[Molecular Formula]

C12H9ClF3NS
[MDL Number]

MFCD03791173
[MOL File]

317318-97-1.mol
[Molecular Weight]

291.72
Chemical PropertiesBack Directory
[Melting point ]

60-62°
[Boiling point ]

363.5±52.0 °C(Predicted)
[density ]

1.357±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[solubility ]

Chloroform, Methanol
[form ]

Solid
[pka]

1.62±0.10(Predicted)
[color ]

Yellow
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Exclamation Mark (GHS07)Health Hazard (GHS08)Environment (GHS09)
GHS05,GHS07,GHS08,GHS09
[Signal word ]

Warning
[Hazard statements ]

H290-H302-H318-H341b-H410
[Precautionary statements ]

P201-P202-P264b-P270-P281-P305+P351+P338-P310-P330-P390-P406b-P501c
[HazardClass ]

IRRITANT
[HS Code ]

2934100090
Hazard InformationBack Directory
[Chemical Properties]

Yellow Solid
[Uses]

Intermediate in the production of GW 501516 and its derivatives
[Synthesis]

2-(4-formyl-2,6-dimethylphenoxy)-2-methylpropanoate

639784-17-1

Triethylamine

121-44-8

Thiazole,5-(chloromethyl)-4-methyl-2-[4-(trifluoromethyl)phenyl]-

317318-97-1

To a stirred solution of Intermediate 1 (8.2 g, 30 mmol) and triethylamine (6.07 g, 8.36 mL, 60 mmol) in anhydrous dichloromethane (120 mL) at 0 °C was slowly added methanesulfonyl chloride (5.49 g, 3.71 mL, 48 mmol). After 2 hours of reaction at 0°C, additional triethylamine (6 mmol) and methanesulfonyl chloride (4.8 mmol) were added. After 2 hours of reaction, thin layer chromatography (TLC, unfolding agent: hexane/ethyl acetate, 1:1) showed complete reaction. The reaction mixture was diluted with dichloromethane (120 mL) and washed sequentially with saturated sodium bicarbonate solution (2 x 240 mL) and water (2 x 240 mL), and the organic phase was dried, filtered, and concentrated to afford 5-(chloromethyl)-4-methyl-2-[4-(trifluoromethyl)phenyl]-1,3-thiazole (8.0 g, 27 mmol, 90% yield) as a yellow solid.

[References]

[1] Patent: WO2004/785, 2003, A2. Location in patent: Page 43
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