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Chemical Structure| 400720-05-0 Chemical Structure| 400720-05-0

Structure of 400720-05-0

Chemical Structure| 400720-05-0

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Product Details of [ 400720-05-0 ]

CAS No. :400720-05-0
Formula : C11H17NO4
M.W : 227.26
SMILES Code : O=C([C@@H]1[C@@]2([H])C[C@@]2([H])CN1C(OC(C)(C)C)=O)O
MDL No. :MFCD08460285
InChI Key :RTWMQNSZCUYSJJ-FXQIFTODSA-N
Pubchem ID :16228665

Safety of [ 400720-05-0 ]

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

Application In Synthesis of [ 400720-05-0 ]

* 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 [ 400720-05-0 ]

[ 400720-05-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 400720-05-0 ]
  • [ 89466-16-0 ]
  • tert-butyl (1S,2S,5R)-2-((6-bromopyridin-2-yl)carbamoyl)-3-azabicyclo[3.1.0]hexane-3-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
To an ice cold solution of (1S,2S,5R)-3-(tert-butoxycarbonyl)-3-azabicyclo[3.1.0]hexane-2-carboxylic acid (103 mg, 0.45 mmole) in 6 mL of CH2Cl2, 1-chloro-N,N,2-trimethylprop-1-en-1-amine (0.07 mL, 1.1 equiv) was added drop-wise with stirring. The stirring was continued for 3 hours at the same temperature. Then <strong>[89466-16-0]6-bromo-3-methylpyridin-2-amine</strong> (93 mg, 1.0 equiv) was added, followed by 0.23 mL (3 equiv) Hunig's base. The cooling bath was removed and the reaction mixture was stirred at room temperature for overnight. The solvent was co-evaporated with 5 mL of MeOH, and the residue was purified by ISCO (eluted 5percent MeOH in DCM, gradient) to obtain 160 mg (90percent) of title compound as yellow oil.
 

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