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Chemical Structure| 1312535-03-7 Chemical Structure| 1312535-03-7

Structure of 1312535-03-7

Chemical Structure| 1312535-03-7

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Product Details of [ 1312535-03-7 ]

CAS No. :1312535-03-7
Formula : C17H19BF3N3O2
M.W : 365.16
SMILES Code : FC(C1=NC(NC2=CC=CC(B3OC(C)(C)C(C)(C)O3)=C2)=NC=C1)(F)F
MDL No. :MFCD28953751

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Application In Synthesis of [ 1312535-03-7 ]

* 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 [ 1312535-03-7 ]

[ 1312535-03-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1312535-03-7 ]
  • [ 405939-39-1 ]
  • [ 1312572-74-9 ]
YieldReaction ConditionsOperation in experiment
27.2% With potassium fluoride; catacxium A;palladium diacetate; In tetrahydrofuran; water; at 75℃; for 17h;Inert atmosphere; A sealable reaction tube was charged with, palladium (II) acetate (6.15 mg, 0.027 mmol), bulyldi-1-adamantylphospliine (19.64 mg, 0.055 mmol) and THF (4 mL) and was stirred for 10 minutes under nitrogen. N-[3-(4,4.5.5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-4- (trifiuoromethyI)pyrimidin-2 -amine (200 mg, 0.548 mmol) (Intermediate VII), r/-butyl (5- bromo-1,3-thiazol-2-yl)carbamate (199 mg, 0.712 mmol), potassium fluoride (95 mg, 1.643 mmol) and Water (1.333 mL) were then successively added. The tube was capped and the mixture was stirred at 75 C for 17 hours, cooled to room temperature and quenched by the addition of 25% aqueous NH4OAC. The aqueous layer was extracted twice with ethyl acetate. The combined organic fractions were washed with water and brine, dried over Na2S04 and concentrated. The product was purified by column chromatography on silica gel (ethyl acetate hexane) to afford fer/-butyl [5-(3-[4-(trifluoromethyl)pyrimidin-2-yl]amino} phenyl)- 1,3- thiazol-2-yl]carbamate (65.1 mg, 27.2 %) as a beige solid. APCI [M+H]+ m/z 382
 

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