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Chemical Structure| 641571-12-2 Chemical Structure| 641571-12-2

Structure of 641571-12-2

Chemical Structure| 641571-12-2

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Product Details of [ 641571-12-2 ]

CAS No. :641571-12-2
Formula : C12H8F3N3
M.W : 251.21
SMILES Code : N#CC1=CC(C(F)(F)F)=CC(N2C=C(C)N=C2)=C1
MDL No. :MFCD10000967
InChI Key :PTMHYQUJHLKUCC-UHFFFAOYSA-N
Pubchem ID :46900393

Safety of [ 641571-12-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 641571-12-2 ]

* 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.

  • Upstream synthesis route of [ 641571-12-2 ]

[ 641571-12-2 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 641571-12-2 ]
  • [ 641571-13-3 ]
YieldReaction ConditionsOperation in experiment
99% With water; sodium hydroxide In 1,4-dioxaneReflux General procedure: General procedure for hydrolysis of nitrile: At a solution of nitrile derivative in dioxane (0.13M) was added NaOH (10 eq, l g/L) in H20. The mixture was heat at reflux overnight. After evaporation of the dioxane, the aqueous layer was washed with AcOEt, then acidified with HCl 2N and extract with AcOEt. The organic layer was dried over Na2S04 filtered and concentrated.
99% With water; sodium hydroxide In 1,4-dioxaneReflux General procedure: General procedure for hydrolysis of nitrile: At a solution of nitrile derivative in dioxane (0,13M) was added NaOH (10 eq, lg/L) in H20. The mixture was heat at reflux overnight. After evaporation of the dioxane, the aqueous layer was washed with AcOEt, then acidified with HCl 2N and extract with AcOEt. The organic layer was dried over Na2S04 filtered and concentrated.
74%
Stage #1: With sodium hydroxide; water In 1,4-dioxane at 100℃;
Stage #2: With hydrogenchloride; water In 1,4-dioxane
Method 27; 3-(4-Methyl-lH-imidazol-l-ylV5-(trifluoromethvπbenzoic acidTo a solution of 3-(4-methyl-lH-imidazol-l-yl)-5-(trifluoromethyl)benzonitrile (Method 26; 180 mg, 0.717 mmol) in 5 ml of dioxane was added 7 ml of a IMNaOH solution. The reaction mixture was allowed to stir overnight at 100 °C. The reaction was cooled to room temperature and quenched by careful addition of concentrated HCl until pH 3 was obtained. The aqueous phase was extracted with EtOAc, dried over Na2SO4, filtered and concentrated under reduced pressure to give 816 mg (74 percent) of the title compound as a yellow solid which was used without further purification, m/z 271.
References: [1] Patent: WO2014/102376, 2014, A1, . Location in patent: Page/Page column 46.
[2] Patent: WO2014/102377, 2014, A1, . Location in patent: Page/Page column 50-51.
[3] Journal of Medicinal Chemistry, 2010, vol. 53, # 15, p. 5439 - 5448.
[4] Patent: WO2006/79791, 2006, A1, . Location in patent: Page/Page column 41.
[5] Patent: WO2004/29038, 2004, A1, . Location in patent: Page 39.
[6] Patent: EP1840122, 2007, A1, . Location in patent: Page/Page column 12.
 

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