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4-(3-BROMO-PHENYL)-THIAZOL-2-YLAMINE

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4-(3-BROMO-PHENYL)-THIAZOL-2-YLAMINE Basic information

Product Name:
4-(3-BROMO-PHENYL)-THIAZOL-2-YLAMINE
Synonyms:
  • BUTTPARK 41\03-41
  • AURORA 22596
  • ART-CHEM-BB B000319
  • 4-(3-BROMO-PHENYL)-THIAZOL-2-YLAMINE
  • 4-(3-BROMOPHENYL)-1,3-THIAZOL-2-AMINE
  • 4-(3-BROMOPHENYL)-1,3-THIAZOLE-2-YLAMINE
  • AKOS B000319
  • AKOS BBS-00008008
CAS:
105512-81-0
MF:
C9H7BrN2S
MW:
255.13
Mol File:
105512-81-0.mol
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4-(3-BROMO-PHENYL)-THIAZOL-2-YLAMINE Chemical Properties

Melting point:
130-131°C
Boiling point:
398.8±17.0 °C(Predicted)
Density 
1.636
storage temp. 
Storage temp. 2-8°C
pka
4.14±0.10(Predicted)
Appearance
White to yellow Solid
CAS DataBase Reference
105512-81-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
HazardClass 
IRRITANT
HS Code 
2934100090
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4-(3-BROMO-PHENYL)-THIAZOL-2-YLAMINE Usage And Synthesis

Application

2-Aminothiazole ring derivatives are an important group of heterocyclic compounds, and 2-amino-4-(3-bromophenyl)thiazole can be used as a pharmaceutical synthesis intermediate. This structure is widely used in the fields of pesticides and pharmaceuticals. Many natural products or small molecule drugs with anti-inflammatory, antitumor, antiviral, and sedative effects contain the 2-aminothiazole ring, making it one of the most frequently constructed functional groups in green drug research in recent years.

Synthesis

2-Amino-4-(3-bromophenyl)thiazole was prepared as follows: in a 25mL reaction vial, 3mL water, 30??L cyclodextrin, 0.50mmol1-bromo-3-ethylbenzene, 1.50mmolNBS and 0.05mmolAIBN were added sequentially and the reaction was carried out at 60??C for 4h. After the reaction was completed, it was cooled and then 1.50mmol sodium bicarbonate and 0.50mmol thiourea were added sequentially. mmol thiourea, and reacted at 80 ?? for 1h, at the end of the reaction, ethyl acetate was added, saturated saline was added to extract, the organic phase was concentrated, and column chromatography yielded 97 mg of white solid 2-amino-4-(3-bromophenyl)thiazole, the yield was 76%.

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