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Chemical Structure| 81529-60-4 Chemical Structure| 81529-60-4

Structure of 81529-60-4

Chemical Structure| 81529-60-4

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Product Details of [ 81529-60-4 ]

CAS No. :81529-60-4
Formula : C12H14N2S
M.W : 218.32
SMILES Code : NC1=NC(C2=C(C)C=C(C)C=C2C)=CS1
MDL No. :MFCD01534593

Safety of [ 81529-60-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 81529-60-4 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 81529-60-4 ]

[ 81529-60-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 4225-92-7 ]
  • [ 17356-08-0 ]
  • [ 81529-60-4 ]
YieldReaction ConditionsOperation in experiment
In ethanol; for 2h;Reflux; 4-Mesitylthiazol-2-amine. 2-Bromo-1-mesitylethanone (2.43 g, 10.1 mmol) and thiourea (0.810 g, 10.6 mmol) were dissolved in 95% ethanol (20 mL). The reaction mixture was heated at reflux for 2.0 h. The solution was concentrated under reduced pressure, and the residue was recrystallized from 2-propanol to give the desired 4-mesitylthiazol-2-amine (2.36 g) as white solids: 1H NMR (500 MHz, CD3OD) delta 7.00 (2H, s), 6.67 (1H, s), 2.31 (3H, s), 2.19 (6H, s).
2.36 g In ethanol; for 2h;Reflux; 2-Bromo-1-mesitylethanone (2.43 g, 10.1 mmol) and thiourea (0.810 g, 10.6 mmol) were dissolved in 95% ethanol (20 mL). The reaction mixture was heated at reflux for 2.0 h. The solution was concentrated under reduced pressure, and the residue was recrystalized from 2-propanol to give the desired 4-mesitylthiazol-2-amine (2.36 g) as white solids: 1H NMR (500 MHz, CD3OD) delta 7.00 (s, 2 H), 6.67 (s, 1 H), 2.31(s, 3 H), 2.19 (s, 6 H).
In ethanol; for 3h;Reflux; General procedure: (iii) A mixture of the above synthetic 9a-10n(calculate to yield 100% for last step, 4 mmol, 1.0 equiv.) and thiourea (4.4 mmol,1.1 equiv.) in anhydrous ethanol (50 mL) was refluxed for 3 h. After that, thesolvent was removed in vacuo andwashed with cold ether. Then the mixture was extracted dichloromethane (3*15mL) and washed with saturated aqueous NaHCO3. The combined organicphases were dried with anhydrous Na2SO4. Then removingthe solvent, the residue was purified by silica gel column (hexane/EtOAc=8:1 to4:1) and dried under vacuum to give 4-arylthiazol-2-amine 10a-10n, yieldwas 50~90%.
 

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