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Chemical Structure| 1314960-42-3 Chemical Structure| 1314960-42-3

Structure of 1314960-42-3

Chemical Structure| 1314960-42-3

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Product Details of [ 1314960-42-3 ]

CAS No. :1314960-42-3
Formula : C6H8FN3
M.W : 141.15
SMILES Code : CC1=CC(F)=CN=C1NN
MDL No. :MFCD10000087

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Application In Synthesis of [ 1314960-42-3 ]

* 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 [ 1314960-42-3 ]

[ 1314960-42-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1314960-42-3 ]
  • [ 475-11-6 ]
  • [ 1443245-52-0 ]
YieldReaction ConditionsOperation in experiment
56% With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20℃; for 18h;Inert atmosphere; c. (S)-l-Methyl-pyrrolidine-2-carboxylic acid N'-(5-fluoro-3-methyl- pyridin-2-yl)-hydrazide (Interme A solution of Intermediate 105b (76 mg, 0.537 mmol), (S)-l-methyl- pyrrolidine-2-carboxylic acid (55 mg, 0.72 mmol) and HOBT (8 mg, 0.72 mmol) in anhydrous DCM (5 mL) was treated with EDC (138 mg, 0.717 mmol) and stirred at RT under a nitrogen atmosphere for 18 h. The reaction mixture was diluted with DCM and washed with brine. The organic layer was dried (MgSO4) and concentrated in vacuo. The resultant residue was purified by FCC on silica, using a gradient of 1-10% MeOH in DCM, to afford the title compound (76 mg, 56%). NM (400 MHz, CDC13): 1.74-2.05 (3H, m), 2.15-2.33 (4H, m), 2.34- 2.46 (1H, m), 2.52 (3H, s), 3.02-3.12 (1H, m), 3.15-3.25 (1H, m), 6.70 (1H, s), 7.08-7.18 (1H, m), 7.90 (1H, d, J = 2.8 Hz), 9.52 (1H, br s).
 

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