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Chemical Structure| 1402889-86-4 Chemical Structure| 1402889-86-4

Structure of 1402889-86-4

Chemical Structure| 1402889-86-4

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Product Details of [ 1402889-86-4 ]

CAS No. :1402889-86-4
Formula : C12H19BrN2O2S
M.W : 335.26
SMILES Code : O=S(C1=C(C)N(CC2CCCCC2)C(Br)=C1)(N)=O

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Application In Synthesis of [ 1402889-86-4 ]

* 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 [ 1402889-86-4 ]

[ 1402889-86-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1402889-86-4 ]
  • [ 197223-39-5 ]
  • [ 1402888-12-3 ]
YieldReaction ConditionsOperation in experiment
28% With potassium carbonate;(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In N,N-dimethyl-formamide; at 120℃; for 16h;Inert atmosphere; Step 5:1-(Cyclohexylmethyl)-5-(3,5-di-tert-butylphenyl)-2-methyl-1H-pyrrole-3-sulfonamide (1)The solution of compound 1d (3.0 g, 9.0 mmol), <strong>[197223-39-5](3,5-di-tert-butylphenyl)boronic acid</strong> (4.2 g, 18 mmol), PdCl2(dppf)2 (300 mg) and K2CO3 (2.8 g, 27 mmol) in 80 mL of DMF was heated at 120°C under N2 atmosphere for 16 h.The resulting solution was concentrated under reduced pressure, diluted with water and extracted with EA twice.The combined organic layers were washed with brine, dried over Na2SO4, filtered, concentrated under reduced pressure and purified by CC (PE:EA = 4:1) to give compound 1 (1.13 g, 28percent) as a white solid.1H NMR (300 MHz, DMSOd6): delta 0.63-0.67 (m, 2H), 0.90-0.98 (m, 3H), 1.22-1.26 (m, 3H), 1.31 (s, 18H), 1.44-1.51 (m, 3H), 2.43 (s, 3H), 3.76 (d, J = 6.9 Hz, 2H), 6.28 (s, 1H), 6.90 (s, 2H), 7.14 (d, J = 1.5 Hz, 2H), 7.38-7.39 (m, 1H); LCMS (mobile phase: 80percent-95percent Acetonitrile-2.5 mmol NH4Ac) purity is 97.2percent, Rt = 2.4 min; MS Calcd.: 444; MS Found: 445 (M+1).
28% With potassium carbonate;(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In N,N-dimethyl-formamide; at 120℃; for 16h;Inert atmosphere; Step 5: 1-(Cvclohexylmethyl)-5-(3.5-di-tert-butylphenyl)-2-methyl-1 H-pyrrole-3-sulfonamide (1)The solution of compound 1d (3.0 g, 9.0 mmol), (3,5-di-ferf-butylphenyl)boronic acid (4.2 g, 18 mmol), Pd(dppf)CI2 (300 mg) and K2C03 (2.8 g, 27 mmol) in DMF (80 mL) was heated at 120°C under N2 for 16 h. The resulting solution was concentrated, diluted with water and extracted with EA twice. The combined organic layers were washed with brine, dried over Na2S0 , filtered, concentrated and purified by CC (PE EA = 4/1) to give compound 1 (1.13 g, 28percent) as a white solid. 1H-NMR (300 MHz, DMSO-d6) delta: 0.63-0.67 (m, 2H), 0.90-0.98 (m, 3H), 1.22-1.26 (m, 3H), 1.31 (s, 18H), 1.44-1.51 (m, 3H), 2.43 (s, 3H), 3.76 (d, J = 6.9 Hz, 2H), 6.28 (s, 1 H), 6.90 (s, 2H), 7.14 (d, J = 1.5 Hz, 2H), 7.38-7.39 (m, 1 H). MS Calcd.: 444; MS Found: 445 (M+1).
 

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