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Chemical Structure| 265324-26-3 Chemical Structure| 265324-26-3

Structure of 265324-26-3

Chemical Structure| 265324-26-3

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Product Details of [ 265324-26-3 ]

CAS No. :265324-26-3
Formula : C7H9N3
M.W : 135.17
SMILES Code : NC1=NC(C2CC2)=NC=C1
MDL No. :MFCD11043794

Safety of [ 265324-26-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 265324-26-3 ]

* 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 [ 265324-26-3 ]

[ 265324-26-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 57297-29-7 ]
  • [ 920-37-6 ]
  • [ 265324-26-3 ]
YieldReaction ConditionsOperation in experiment
27% With triethylamine; In ethanol; for 1h;Reflux; Example 196a 2-cyclopropylpyrimidin-4-amine 196a Cyclopropylcarbamidine hydrochloride (1.0 g, 8.3 mmol) was dissolved in ethanol (25 mL) and triethylamine (1.26 g, 12.5 mmol), followed by the addition of 2-chloroacrylonitrile (870 mg, 10 mmol). The resulting orange-yellow solution was refluxed for 1h. The mixture was cooled to room temperature and filtered. The filtrate was concentrated in vacuo and the residue was purified by reverse-phase Combiflash to afford 196a (300 mg, 27percent) as a light brown solid. MS-ESI: [M+H]+ 136
With triethylamine; In ethanol; for 0.5h;Heating / reflux;Product distribution / selectivity; Alternative Preparation Method for Step A]: Cyclopropylcarbamidine hydrochloride (7.61 g) was dissolved in ethanol (125 mL) and triethylamine (19.35 mL) and 2-chloro-acrylonitrile (5.52 mL) were added. The resulting orange-yellow solution was refluxed for 30 minutes. The mixture was cooled and left in a refrigerator over night. The solid was removed by filtration and the filtrate was concentrated in vacuo. The residue was purified by flash chromatography (ethyl acetate/methanol 9:1) to give 2-cyclopropyl-pyrimidin-4-ylamine (4.2 g) as a light brown solid that was still contaminated with an unidentified component, but used without further purification. 1H NMR (delta, DMSO-d6, product signals only): 7.88 (d, 1H), 6.64 (br s, 2H), 6.16 (d, 1H), 1.89-1.82 (m, 1H), 0.87-0.81 (m, 4H).
  • 2
  • [ 61310-53-0 ]
  • [ 57297-29-7 ]
  • [ 265324-26-3 ]
YieldReaction ConditionsOperation in experiment
85.0% 2-Cyclopropylpyrimidin-4-amine A suspension of cyclopropylcarbamidine hydrochloride (1.0 g, 8.3 mmol) in sodium methoxide (0.5 M in MeOH, 16.6 mL, 8.3 mmol) was allowed to stir at rt for 30 min. The mixture was then filtered and concentrated. Ethoxyacrylonitrile (0.85 mL, 8.3 mmol) was added and the reaction was allowed to stir at 135° C. for 3 h, then allowed to cool to rt and stir for another 16 h. The reaction was concentrated and the crude product was purified by column chromatography to provide 2-cyclopropylpyrimidin-4-amine (1.10 g, 85.0percent) as a solid. LCMS (FA): m/z=136.2 (M+H).
 

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