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Chemical Structure| 1246960-25-7 Chemical Structure| 1246960-25-7

Structure of 1246960-25-7

Chemical Structure| 1246960-25-7

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Product Details of [ 1246960-25-7 ]

CAS No. :1246960-25-7
Formula : C18H16F3NO3
M.W : 351.32
SMILES Code : O=C(O)C[C@H](C(NCC1=CC=CC=C1)=O)CC2=CC(F)=C(F)C=C2F

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Application In Synthesis of [ 1246960-25-7 ]

* 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 [ 1246960-25-7 ]

[ 1246960-25-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1246960-25-7 ]
  • [ 486460-21-3 ]
  • [ 1242069-63-1 ]
YieldReaction ConditionsOperation in experiment
86% With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; for 4h;Inert atmosphere; To a solution of the acid (VII?) (300 mg, 0.90 mmol) and triazolopiperazine (VIII) (170 mg, 0.90 mmol) in CH2Cl2 (10 mL) is added N-hydroxybenzotriazole (150 mg, 1.08 mmol), and 10 minutes later, EDC (260 mg, 1.35 mmol). The mixture, under an inert atmosphere of N2, is magnetically stirred for 4 hours until completion, then a saturated solution of sodium bicarbonate (5 mL) is added and the mixture is extracted with dichloromethane. The combined organic phases are dried and evaporated under reduced pressure. The product is purified by flash chromatography, obtaining 406 mg (86% yield) of a crystalline white solid, compound (IX?). 1H NMR (300 MHz, d6-dmso, 100 C.) delta 7.4-7.2 (m, 7H), 6.90 (bs, 1H) 4.97 & 4.90 (AB system, J=12.9 Hz, 2×1H), 4.92 (s, 2H), 4.26-4.14 (m, 3H), 3.97 (t, J=5.5 Hz, 2H), 2.92 & 2.67 (2×dd, J=14.1, 4.9 Hz, 2×1H), 2.83-2.72 (m, 2H).
EXAMPLE 6ATo a solution of the acid (VII') (300 mg, 0.90 mmol) and triazolopiperazine (VIII) (170 mg, 0.90 mmol) in CH2CI2 (10 mL) is added /V-hydroxybenzotriazole (150 mg, 1 .08 mmol), and 10 minutes later, EDC (260 mg, 1 .35 mmol). The mixture, under an inert atmosphere of N2, is magnetically stirred for 4 hours until completion, then a saturated solution of sodium bicarbonate (5 mL) is added and the mixture is extracted with dichloromethane.The combined organic phases are dried and evaporated under reduced pressure. The product is purified by flash chromatography, obtaining 406 mg (86% yield) of a crystalline white solid, compound (IX').1 H NMR (300 MHz, d6-dmso, 100 C) delta 7.4-7.2 (m, 7H), 6.90 (bs, 1 H) 4.97 & 4.90 (AB system, J= 12.9 Hz, 2 x 1 H), 4.92 (s, 2H), 4.26-4.14 (m, 3H), 3.97 (t, J=5.5 Hz, 2H), 2.92 & 2.67 (2 x dd, J=14.1 , 4.9 Hz, 2 x 1 H), 2.83-2.72 (m, 2H).
 

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