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Chemical Structure| 134003-02-4 Chemical Structure| 134003-02-4

Structure of 134003-02-4

Chemical Structure| 134003-02-4

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Product Details of [ 134003-02-4 ]

CAS No. :134003-02-4
Formula : C6H9NO
M.W : 111.14
SMILES Code : O=C1N[C@]2([H])CC[C@@]1([H])C2
MDL No. :MFCD01320868

Safety of [ 134003-02-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 134003-02-4 ]

* 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 [ 134003-02-4 ]

[ 134003-02-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 24424-99-5 ]
  • [ 134003-02-4 ]
  • [ 151907-79-8 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; In methanol; The preparation method is described in: J. Med. Chem. 2001, 44, 4379-4392. Specific operations are as follows: Starting from the chiral starting material (1R,4S)-6, added hydrochloric acid methanol solution and (Boc)2O protection to give compound 7; Compound 7 was subjected to 3+2 cycloaddition to give compound 8; Compound 8 was subjected to hydrogenolysis to give compound 9; The compound 9 was subjected to acetylation reaction to give compound 10; Compound 10, t-butyloxycarbonyl group was removed by a solution of hydrochloric acid in diethyl ether to obtain compound I.
 

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