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Chemical Structure| 59083-39-5 Chemical Structure| 59083-39-5

Structure of 59083-39-5

Chemical Structure| 59083-39-5

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Product Details of [ 59083-39-5 ]

CAS No. :59083-39-5
Formula : C12H17N
M.W : 175.27
SMILES Code : CC1=CC=C(C=C1)C1CCNCC1
MDL No. :MFCD03839928

Safety of [ 59083-39-5 ]

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

Application In Synthesis of [ 59083-39-5 ]

* 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 [ 59083-39-5 ]

[ 59083-39-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 401564-36-1 ]
  • [ 59083-39-5 ]
  • 3-{(2S,4S)-1-tert-butoxycarbonyl-4-[4-(p-tolyl)piperidino]-2-pyrrolidinylcarbonyl}-1,3-thiazolidine [ No CAS ]
YieldReaction ConditionsOperation in experiment
With sodium tris(acetoxy)borohydride; acetic acid; In water; 1,2-dichloro-ethane; (1) The title compound (504 mg) of Reference Example 12, 4-(p-tolyl)piperidine (353 mg) and acetic acid (0.096 mL) were dissolved in 1,2-dichloroethane (10 mL), and sodium triacetoxyborohydride (710 mg) was added thereto. The mixture was stirred at room temperature for 18 hr. The reaction mixture was added to water and the mixture was extracted with chloroform. The extract was washed with brine and dried. The solvent was evaporated under reduced pressure to give 3-{(2S,4S)-1-tert-butoxycarbonyl-4-[4-(p-tolyl)piperidino]-2-pyrrolidinylcarbonyl}-1,3-thiazolidine (115 mg) as a whitesolid.
 

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