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Chemical Structure| 179557-01-8 Chemical Structure| 179557-01-8

Structure of 179557-01-8

Chemical Structure| 179557-01-8

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Product Details of [ 179557-01-8 ]

CAS No. :179557-01-8
Formula : C13H24N2O2
M.W : 240.34
SMILES Code : CC(C)(C)OC(=O)N1CCC(CC1)NC1CC1
MDL No. :MFCD03426074
InChI Key :GERLYNRROAQLRS-UHFFFAOYSA-N
Pubchem ID :2769591

Safety of [ 179557-01-8 ]

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

Application In Synthesis of [ 179557-01-8 ]

* 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 [ 179557-01-8 ]

[ 179557-01-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 57684-71-6 ]
  • [ 179557-01-8 ]
  • tert-butyl 4-[cyclopropyl(1,2-oxazol-3-ylmethyl)amino]piperidine-1-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
58% Intermediate 11, tert-butyl 4-(cyclopropylamino)piperid me-i -carboxylate (200 mg, 0.83 mmol) was dissolved in ethanol (10 mL) and sodium bicarbonate (200 mg, 2.38 mmol) was added. The reaction mixture was stirred at 0 C for 30 mm, then Intermediate 14, 3-(chloromethyl)-1 2- oxazole (97 mg, 0.83 mmol) was added dropwise at it The resulting reaction mixture wasstirred at 60 C for 16 h. The solvents were removed in vacuo and the residue was partitioned between H20 (120 mL) and EtOAc (100 mL). The aqueous layer was further extracted with EtOAc (2 x 100 mL) and the combined organic layers were dried (Na2SO4), and the solvents were removed in vacuo. The residue was purified by column chromatography (normal basic activated alumina, 0.5 % to 1 .0 % MeOH in DCM) to give tert-butyl 4-[cyclopropyl(1 ,2-oxazol-3-ylmethyl)amino]piperidine-1-carboxylate (150 mg, 58 %) as a liquid. LCMS (Method I): mlz 322 [M+H] (ES), at 4.92 mi UV active
 

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