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Chemical Structure| 124400-52-8 Chemical Structure| 124400-52-8

Structure of 124400-52-8

Chemical Structure| 124400-52-8

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Product Details of [ 124400-52-8 ]

CAS No. :124400-52-8
Formula : C14H12N2O2S
M.W : 272.32
SMILES Code : NC1=CC2=C(N(S(=O)(C3=CC=CC=C3)=O)C=C2)C=C1

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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 [ 124400-52-8 ]

[ 124400-52-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 98556-31-1 ]
  • [ 124400-52-8 ]
  • [ 287193-15-1 ]
YieldReaction ConditionsOperation in experiment
In tert-butyl alcohol; (1-Benzenesulfonyl-1H-indol-5-yl)-(6-iodo-quinazolin4-yl)-amine (20) 6-iodo-4-chloroquinazoline 13 (2.38 g, 8.20 mmol) and 5-amino-1-benzenesulfonylindole 21 (2.46 g, 9.00 mmol) were combined in DCE (20 mL) and t-butanol (20 mL). The resulting mixture was heated at reflux under nitrogen for 18 hours to form a bright yellow suspension. Upon cooling the solids were filtered and rinsed with CH2Cl2 and placed under high vacuum to remove any excess solvent. The title compound (3.23 g, 75%) was obtained as a yellow solid. For compound 20: 1H NMR (DMSO-d6; 400 MHz): δ: 10.05 (s, 2H,), 8.93 (s, 1H), 8.53 (s, 1H), 8.25 (m, 1H,), 8.10 (m, 5H), 7.97 (m, 3H), 7.82 (m, 2H), 7.70 (m, 2H), 7.65 (m, 2H), 6.88 (d, 1H, J=3.57 Hz).
In tert-butyl alcohol; (1-Benzenesulfonyl-1H-indol-5-yl)-(6-iodo-quinazolin-4-yl)-amine (14): 6-iodo-4-chloroquinazoline (2.38 g, 8.20 mmol) and 5-amino-1-benzenesulfonylindole (2.46 g, 9.00 mmol) were combined in DCE (20 mL) and t-butanol (20 mL). The resulting mixture was heated at reflux under nitrogen for 18 hours to form a bright yellow suspension. Upon cooling the solids were filtered and rinsed with CH2Cl2 and placed under high vacuum to remove any excess solvent. Quinazoline 14 (3.23 g, 75%) was obtained as a yellow solid. 1H NMR (DMSO d6; 400 MHz): δ: 9.24 (s, 1H, NH), 8.84 (s, 1H), 8.33 (dd, 1H, 8.9 Hz, 1.7 Hz), 8.01 (m, 4H), 7.90 (m, 2H), 7.70 (m, 2H), 7.60 (m, 3H), 6.92 (dd, 1H, J=3.7 Hz, 0.6 Hz).
 

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