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Chemical Structure| 955368-93-1 Chemical Structure| 955368-93-1

Structure of 955368-93-1

Chemical Structure| 955368-93-1

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Product Details of [ 955368-93-1 ]

CAS No. :955368-93-1
Formula : C9H12N4OS
M.W : 224.28
SMILES Code : O=C1N(C(C)C)NC2=NC(SC)=NC=C21

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Application In Synthesis of [ 955368-93-1 ]

* 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 [ 955368-93-1 ]

[ 955368-93-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 638218-78-7 ]
  • [ 955368-93-1 ]
  • 1-[6-(2-hydroxypropan-2-yl)pyridin-2-yl]-6-(methylsulfanyl)-2-(propan-2-yl)-1H,2H,3H-pyrazolo[3,4-d]pyrimidin-3-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
31.2% With copper(l) iodide; potassium carbonate; N,N`-dimethylethylenediamine; In 1,4-dioxane; at 95℃; for 12h; Into a lOO-mL round-bottom flask, was placed <strong>[638218-78-7]2-(6-bromopyridin-2-yl)propan-2-ol</strong> (5.78 g, 26.750 mmol, 3.00 equiv), 6- (methylsulfanyl)-2-(propan-2-yl)-lH,2H,3H-pyrazolo[3,4-d]pyrimidin-3-one (2 g, 8.917 mmol, 1 equiv), methyl[2-(methylamino)ethyl]amine (0.79 g, 8.917 mmol, 1 equiv), Cul (1.70 g, 8.917 mmol, 1 equiv), K2C03 (3.70 g, 26.752 mmol, 3 equiv), Dioxane (30 mL). The resulting solution was stirred for 12 hr at 95C. The solids were filtered out. The resulting mixture was concentrated. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (0: 1-2: 1). This resulted in 1 g (31.20%) of l-[6-(2-hydroxypropan-2- yl)pyridin-2-yl]-6-(methylsulfanyl)-2-(propan-2-yl)-lH,2H,3H-pyrazolo[3,4-d]pyrimidin-3- one as a white solid. LC-MS-5: [M+l]=360, 1H-NMR-5: (300MHz, CDCl3, ppm): d 8.89(s, 1H), 7.96-7.9l(m, 1H), 7.72-7.70(m, 1H), 7.74-7.42(m, 1H), 4.35-4.30(m, 1H), 2.57(s, 3H), l.64(s, 6H), l.54-l.52(m, 6H).
55 mg With copper(l) iodide; potassium carbonate; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; at 80℃; for 12h; Step-6: Synthesis of 1-(6-(2-hydroxypropan-2-yl)pyridin-2-yl)-2-isopropyl-6-(methylthio)-1,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one To a stirred solution of 2-isopropyl-6-(methylthio)-1,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one (0.26 g, 1.16 mmol, 1.0 eq) and <strong>[638218-78-7]2-(6-bromo-2-pyridyl)propan-2-ol</strong> (0.3 g, 1.39 mmol, 1.20 eq) in dioxane (10 mL) were added CuI (0.044 g, 0.23 mmol, 1.0 eq), K2CO3 (0.32 g, 2.32 mmol, 2 eq) and DIPEA (0.041 g, 0.46 mmol, 0.4 eq) and stirred at 80 C. 12 h. After completion of reaction, solvent was removed under reduced pressure; residue was diluted with water and extracted with ethyl acetate (10 mL*3). Combined organic layer was washed with brine solution, dried over anhydrous sodium sulphate and concentrated under reduced pressure to afford crude product, which was purified by flash chromatography to afford 1-(6-(2-hydroxypropan-2-yl)pyridin-2-yl)-2-isopropyl-6-(methylthio)-1,2-dihydro-3H-pyrazolo[3,4-d]pyrimidin-3-one (55 mg, 13+%) as yellow oil.
 

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