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Chemical Structure| 5751-17-7 Chemical Structure| 5751-17-7

Structure of 5751-17-7

Chemical Structure| 5751-17-7

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Product Details of [ 5751-17-7 ]

CAS No. :5751-17-7
Formula : C8H12N2OS
M.W : 184.26
SMILES Code : O=C1NC(SC)=NC(CCC)=C1
MDL No. :MFCD00847268

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Application In Synthesis of [ 5751-17-7 ]

* 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 [ 5751-17-7 ]

[ 5751-17-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 5751-17-7 ]
  • [ 50670-64-9 ]
  • [ 1394321-71-1 ]
YieldReaction ConditionsOperation in experiment
at 160℃; A mixture of 2-(methylthio)-6-propylpyrimidin-4(3H)-one (5 g, 27.1 mmol) prepared in Step 1 of Preparation 1 and <strong>[50670-64-9]5-amino-2-methylbenzonitrile</strong> (7 g, 53 mmol) was stirred at 160C overnight. The reaction mixture was cooled to room temperature and then ethanol (30 ml) was added thereto. The reaction mixture was stirred for 1 hour and then filtered to give 6.3g of the titled compound as a pale yellow solid.[658] 1H-NMR(400MHz, CD3OD) delta 8.12(d, 1H), 7.70-7.60(m, 1H), 7.35(d, 1H), 5.80(s, 1H), 2.50-2.40(m, 5H), 1.73(q, 2H), 0.99(t, 3H)
at 160℃; A mixture of 2-(methylthio)-6-propylpyrimidin-4(3H)-one (5 g, 27.1 mmol) prepared in Step 1 of Preparation 1 and <strong>[50670-64-9]5-amino-2-methylbenzonitrile</strong> (7 g, 53 mmol) was stirred at 160C overnight. The reaction mixture was cooled to room temperature and then ethanol (30 ml) was added thereto. The reaction mixture was stirred for 1 hour and then filtered to give 6.3 g of the titled compound as a pale yellow solid.[598] 1H-NMR(400MHz, CD3OD) delta 8.12(d, 1H), 7.70-7.60(m, 1H), 7.35(d, 1H), 5.80(s, 1H), 2.50-2.40(m, 5H), 1.73(q, 2H), 0.99(t, 3H)
6.3 g at 160℃; A mixture of 2-(methylthio)-6-propylpyrimidin-4(3H)-one (5 g, 27.1 mmol) prepared in Step 1 of Preparation 1 and <strong>[50670-64-9]5-amino-2-methylbenzonitrile</strong> (7 g, 53 mmol) was stirred at 160 C. overnight. The reaction mixture was cooled to room temperature and then ethanol (30 ml) was added thereto. The reaction mixture was stirred for 1 hour and then filtered to give 6.3 g of the titled compound as a pale yellow solid. [0525] 1H-NMR (400 MHz, CD3OD) delta 8.12 (d, 1H), 7.70-7.60 (m, 1H), 7.35 (d, 1H), 5.80 (s, 1H), 2.50-2.40 (m, 5H), 1.73 (q, 2H), 0.99 (t, 3H)
 

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