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Chemical Structure| 1221432-10-5 Chemical Structure| 1221432-10-5

Structure of 1221432-10-5

Chemical Structure| 1221432-10-5

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Product Details of [ 1221432-10-5 ]

CAS No. :1221432-10-5
Formula : C11H9N3S
M.W : 215.27
SMILES Code : N#CC1=C(N)SC(CC2=NC=CC=C2)=C1

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Application In Synthesis of [ 1221432-10-5 ]

* 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 [ 1221432-10-5 ]

[ 1221432-10-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1221432-10-5 ]
  • [ 68776-60-3 ]
  • 2-oxazol-2-yl-6-pyridin-2-ylmethyl-thieno[2,3-d]pyrimidin-4-ylamine hydrochloride [ No CAS ]
YieldReaction ConditionsOperation in experiment
Solid t-BuOK (9 mg, 0.08 mmol) was added to a dioxane suspension (0.20 mL) of 2- amino-5-pyridin-2-ylmethyl-thiophene-3-carbonitrile (87 mg, 0.40 mmol) and oxazole-2- carbonitrile (46 mg, 0.49 mmol, prepared as an intermeduiate in Example 2) and the mixture was heated by microwave irradiation (130 0C, 10 min, 300 W). The reaction mixture was diluted with dichloromethane and methanol, dry packed onto silica gel, and purified via column chromatography to give 107 mg of the title compound. The free base was dissolved in CH2Cl2 containing a minimal amount of methanol to achieve solution and the solution was added to 1 M HCl in Et2O. The precipitated hydrochloride salt was collected by vacuum filtration to give 112 mg of the title compound. 1H NMR (300 MHz, DMS0-D6) delta ppm 8.89 (d, J=4.9 Hz, 1 H), 8.53 (t, J=I .1 Hz, 1 H), 8.31 (s, 1 H), 7.92 - 8.18 (m, 4 H), 7.51 (s, 1 H), 7.48 (s, IH), 4.80 (s, 2 H); MS m/e 310 (M+H).
 

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