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Structure of 515824-43-8

Chemical Structure| 515824-43-8

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Product Details of [ 515824-43-8 ]

CAS No. :515824-43-8
Formula : C6H5ClF3N3
M.W : 211.57
SMILES Code : FC(C1=CN=C(Cl)N=C1NC)(F)F
MDL No. :MFCD22056179
InChI Key :DBZWBBJKHCGBCI-UHFFFAOYSA-N
Pubchem ID :21077587

Safety of [ 515824-43-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 515824-43-8 ]

* 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 [ 515824-43-8 ]

[ 515824-43-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 515824-43-8 ]
  • [ 41608-73-5 ]
  • [ 1441720-56-4 ]
YieldReaction ConditionsOperation in experiment
20% With trifluoroacetic acid; In butan-1-ol; at 100.0℃; for 1.5h;Sealed tube; Example 1 : N2-(2-Methoxy-4-(methylsulfonyl)phenyl)-N4-methyl-5- (trifLuoromethyl)pyrimidine-2,4-diamine To a mixture of <strong>[41608-73-5]2-methoxy-4-(methylsulfonyl)aniline</strong> (0.095 g, 0.47 mmol) and 2- chloro-N-methyl-5-(trifluoromethyl)pyrimidin-4-amine (0.10 g, 0.47 mmol) in 1-butanol (1.5 mL) was added TFA (0.036 mL, 0.047 mmol). The reaction was stirred in a sealed tube at 100 °C for 1.5 h. The reaction was concentrated and the product was isolated by reverse-phase HPLC to give N2-(2-methoxy-4-(methylsulfonyl)phenyl)-N4-methyl-5- (trifluoromethyl)pyrimidine-2,4-diamine (0.18 g, 20percent). 1H NMR (400 MHz, DMSO) ? 8.58 (d, J = 12.9, 1H), 8.24 (d, J = 5.0, 2H), 7.53 (d, J = 10.1, 1H), 7.48 (s, 1H), 7.38 - 7.29 (m, 1H), 3.99 (s, 3H), 3.20 (s, 3H), 2.94 (d, J = 4.3, 3H); LRRK2 Ki = 0.002.
  • 2
  • [ 515824-43-8 ]
  • [ 1441723-24-5 ]
  • [ 1441720-69-9 ]
YieldReaction ConditionsOperation in experiment
With trifluoroacetic acid; In butan-1-ol; at 75.0℃; for 2.0h;Sealed tube; Example 3: 2-Fluoro-5-methoxy-4-(4-(methylamino)-5- (trifLuoromethyl)pyrimidin-2-ylamino)benzonitrile To a mixture of <strong>[1441723-24-5]4-amino-2-fluoro-5-methoxybenzonitrile</strong> (66 mg, 0.40 mmol) and 2-chloro-N-methyl-5-(trifluoromethyl)pyrimidin-4-amine (0.10 g, 0.47 mmol) in 1- butanol (2 mL) was added TFA (0.05 mL, 0.07 mmol). The reaction was stirred in a sealed tube at 75 C for 2 h. The reaction was concentrated and the product was isolated by reverse-phase HPLC to give 2-fluoro-5-methoxy-4-(4-(methylamino)-5- (trifluoromethyl)pyrimidin-2-ylamino)benzonitrile. 1H NMR (400 MHz, DMSO) ? 8.57 (d, J = 13.4, 2H), 8.34 (s, 1H), 8.29 (d, J = 6.1, 1H), 7.56 - 7.42 (m, 3H), 3.93 (s, 3H), 2.95 (s, 3H); LRRK2 Ki = 0.022.
 

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