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Chemical Structure| 1141016-83-2 Chemical Structure| 1141016-83-2

Structure of 1141016-83-2

Chemical Structure| 1141016-83-2

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Product Details of [ 1141016-83-2 ]

CAS No. :1141016-83-2
Formula : C12H21N3O
M.W : 223.31
SMILES Code : NC1=CC(C(C)(C)C)=NN1C[C@@H]2OCCC2

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* 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 [ 1141016-83-2 ]

[ 1141016-83-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 207981-46-2 ]
  • [ 1141016-83-2 ]
  • [ 1140917-50-5 ]
YieldReaction ConditionsOperation in experiment
Example 10D N-{3-tert-butyl-1-[(2R)-tetrahydrofuran-2-ylmethyl]-1H-pyrazol-5-yl}-2-fluoro-5-(trifluoromethyl)benzamide To a solution of the product of Example 10C (7.8 g, 35.0 mmol) and triethylamine (14.6 mL, 105 mmol) in THF (60 mL) at ambient temperature was added <strong>[207981-46-2]2-fluoro-5-(trifluoromethyl)benzoyl chloride</strong> (5.3 mL, 35.0 mmol) dropwise over 10 min. The mixture was stirred at ambient temperature for 3 h. The mixture was quenched with saturated, aqueous NaHCO3(20 mL) and diluted with EtOAc (20 mL). The layers were separated and the aqueous layer was extracted with EtOAc (3*10 mL). The combined organics were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. Purification by column chromatography (SiO2, 40% hexanes/EtOAc) gave the title compound (11.0 g, 26.6 mmol, 76% yield). MS (DCI/NH3) m/z 414 (M+H)+.
660 mg With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 20℃; for 4h;Inert atmosphere; To a solution of 2-fluoro-5-trifluoromethylbenzoic acid (500 mg, 2.4 mmol) in anhydrous dichloromethane (10 mL) was added oxalyl chloride (410 μL, 4.8 mmol) followed by N,N-dimethylformamide (2 drops) and the mixture was stirred at room temperature for 3 hours. The volatiles were removed under a stream of nitrogen and the residue taken up in dichloromethane and added slowly to a solution of 11 (540 mg, 2.4 mmol) and N,N-diisopropylethylamine (1.0 mL, 6.0 mmol) in dichloromethane (10 mL) at 0 C. The mixture was warmed to room temperature and stirred for 4 hours. The mixture was diluted with dichloromethane (30 mL) and washed with saturated aqueous sodium hydrogen carbonate (20 mL) and saturated aqueous ammonium chloride. The organic phase was dried over anhydrous magnesium sulfate, concentrated under reduced pressure and purified by flash column chromatography using ethyl acetate, hexane (0:1 to 3:7) as an eluent to obtain the title compound (660 mg, 67%) as an off-white waxy solid, Rf: 0.45 (2:3 ethyl acetate, hexane); IR (vmax (neat)): 3294, 2962, 1680, 1547, 1326, 1232, 1129, 1092 cm-1; 1H NMR (400 MHz, CDCl3): δ 1.31 (9H, s), 1.62-1.76 (2H, m), 1.80-1.94 (1H, m), 2.00-2.08 (1H, m), 3.68-3.89 (2H, m), 4.11 (1H, dd, J = 15.1, 5.8 Hz), 4.18-4.29 (1H, m), 4.41 (1H, dd, J = 15.4, 1.9 Hz), 6.55 (1H, s), 7.28-7.36 (1H, m), 7.74-7.84 (1H, m), 8.39 (1H, dd, J = 6.9, 2.5 Hz), 10.08 (1H, d, J = 8.1 Hz) ppm; 13C NMR (100 MHz, CDCl3): δ 25.9, 28.1, 30.6, 32.4, 53.0, 68.8, 79.7, 95.6, 117.3 (d, J = 25.3 Hz), 122.4 (d, J = 13.8 Hz), 122.9 (q, J = 272.1 Hz), 128.0 (q, J = 30.3 Hz), 130.1-130.2 (m), 130.7-140.0 (m), 136.4, 159.0 (d, J = 2.8 Hz), 161.0, 161.9 (d, J = 255.2 Hz) ppm; 19F NMR (282 MHz, DMSO-d6): δ -62.3 (CF3), -108.4 (CF) ppm; LRMS (+ESI) m/z: 436.2 ([M+Na]+ 100%), 849.2 ([2M+Na]+ 43%).
 

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