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Chemical Structure| 156339-46-7 Chemical Structure| 156339-46-7

Structure of 156339-46-7

Chemical Structure| 156339-46-7

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Product Details of [ 156339-46-7 ]

CAS No. :156339-46-7
Formula : C8H18N2O
M.W : 158.24
SMILES Code : CC(O)(C)CN1CCNCC1
MDL No. :MFCD10575004
InChI Key :MUIRIPUTKCTCGV-UHFFFAOYSA-N
Pubchem ID :258202

Safety of [ 156339-46-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 156339-46-7 ]

* 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 [ 156339-46-7 ]

[ 156339-46-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 110-85-0 ]
  • [ 558-42-9 ]
  • [ 156339-46-7 ]
YieldReaction ConditionsOperation in experiment
60% In ethanol; at 110℃; for 6h; EXAMPLE 122 {4-[2-tert-Butyl-1-(tetrahydropyran-4-ylmethyl)-1H-imidazol-4-yl]thiophen-2-yl}-[4-(2-hydroxy-2-methylpropyl)piperazin-1-yl]methanone (Compound 122) Step 1; Piperazine (6.88 g, 80.0 mmol) was dissolved in ethanol (40 mL), and 1-chloro-2-methyl-2-propanol (2.18 g, 20.0 mmol) was added thereto, and then, the mixture was stirred at 110°C for 6 hours. After the mixture was left to cool to room temperature, the solvent was evaporated. Then, ethyl acetate was added to the residue, and the precipitated solid was removed by filtration. The solvent of the filtrate was removed under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/methanol = 90/10) to give 2-methyl-1-(piperazin-1-yl)propan-2-ol (1.89 g, 11.96 mmol, 60percent).
at 110℃; for 6h; Piperazine (6.88 g, 80 mmol) was dissolved in ethanol (40 mL).1-Chloro-2-methyl-2-propanol (2.18 g, 20 mmol) was added. The mixture was stirred at 110°C for 6h. After the mixture was left to cool to room temperature, the solvent was evaporated. Ethyl acetate (40 mL) was added and the precipitated solid was removed by filtration. The filtrate was concentrated under reduced pressure to afford 2-methyl-1-piperazin-1-yl-propan-2-ol (4.1 g, crude) as a white solid, which was used directly to the next step without purification. MS (ESI): m/z =159.3 [M+1]+.
 

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