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Chemical Structure| 1124329-94-7 Chemical Structure| 1124329-94-7

Structure of 1124329-94-7

Chemical Structure| 1124329-94-7

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Product Details of [ 1124329-94-7 ]

CAS No. :1124329-94-7
Formula : C11H13ClN4O
M.W : 252.70
SMILES Code : O=C1N(C)C2=CN=C(Cl)N=C2N1C3CCCC3

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Application In Synthesis of [ 1124329-94-7 ]

* 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 [ 1124329-94-7 ]

[ 1124329-94-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1124329-94-7 ]
  • [ 53297-70-4 ]
  • [ 1124329-10-7 ]
YieldReaction ConditionsOperation in experiment
A mixture of <strong>[53297-70-4]4-amino-3-methylbenzenesulfonamide</strong> (0.075 g), 4-methylbenzene-sulfonic acid (0.1 g) and 2-chloro-9-cyclopentyl-7-methyl-purin-8-one (Method 4, 0.075 g) in 4-methyl-2-pentanol (1.5 mL) was heated at 2000C for 5 mins by microwave then cooled to r.t. The reaction was repeated on an identical scale but using 1-butanol (1.5 mL) in place of 4-methyl-2-pentanol. The combined reaction mixtures were purified by SCX, eluting with 2M NH3 in MeOH to give a coloured gum. The gum was purified by reverse phase basic HPLC to afford the title compound (0.05 g, 21%) as a colourless solid; 1H NMR: (CDCl3) 1.69-1.75 (2H, m), 1.96-2.05 (4H, m), 2.26-2.31 (2H, m), 2.40 (3H, s), 3.41 (3H, s), 4.70 (2H, s), 4.79-4.88 (IH, m), 6.98 (IH, d), 7.75 (IH, d), 7.77-7.79 (IH, m), 7.90 (IH, s), 8.54 (IH, d); m/r. MH+ 403; EAA: 1.28; EAA2: 0.0166.
A mixture of <strong>[53297-70-4]4-amino-3-methylbenzenesulfonamide</strong> (0.075 g), 4-methylbenzene-sulfonic acid (0.1 g) and 2-chloro-9-cyclopentyl-7-methyl-purin-8-one (Method 4, 0.075 g) in 4-methyl-2-pentanol (1.5 mL) was heated at 2000C for 5 mins by microwave then cooled to r.t. The reaction was repeated on an identical scale but using 1-butanol (1.5 mL) in place of 4-methyl-2-pentanol. The combined reaction mixtures were purified by SCX, eluting with 2M NH3 in MeOH to give a coloured gum. The gum was purified by reverse phase basic HPLC to afford the title compound (0.05 g, 21%) as a colourless solid; 1H NMR: (CDCl3) 1.69-1.75 (2H, m), 1.96-2.05 (4H, m), 2.26-2.31 (2H, m), 2.40 (3H, s), 3.41 (3H, s), 4.70 (2H, s), 4.79-4.88 (IH, m), 6.98 (IH, d), 7.75 (IH, d), 7.77-7.79 (IH, m), 7.90 (IH, s), 8.54 (IH, d); m/r. MH+ 403; EAA: 1.28; EAA2: 0.0166.
 

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