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Chemical Structure| 1212974-29-2 Chemical Structure| 1212974-29-2

Structure of 1212974-29-2

Chemical Structure| 1212974-29-2

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Product Details of [ 1212974-29-2 ]

CAS No. :1212974-29-2
Formula : C11H13NO2
M.W : 191.23
SMILES Code : O=C(C1=CC2=C(CC[C@H]2N)C=C1)OC
MDL No. :MFCD09256284

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Application In Synthesis of [ 1212974-29-2 ]

* 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 [ 1212974-29-2 ]

[ 1212974-29-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1077-58-3 ]
  • [ 1212974-29-2 ]
  • [ 1365151-96-7 ]
  • 2
  • [ 1077-58-3 ]
  • [ 1212974-29-2 ]
  • [ 1365150-20-4 ]
YieldReaction ConditionsOperation in experiment
57% (R)-Methyl 3-(2-tert-butylbenzamido)-2,3-dihydro-1H-indene-5-carboxylate (B-27) 2-tert-Butylbenzoic acid (0.75 g, 4.2 mmol, 1 eq) was dissolved in dichloromethane (40 ml), and at 0 C. HATU (1.5 g, 4.2 mmol, 1 eq) and DIPEA (1.7 ml, 10.52 mmol, 2.5 eq) were added and stirring was carried out for 30 min. Then (R)-methyl 3-amino-2,3-dihydro-1H-indene-5-carboxylate (A-07) (804 mg, 4.2 mmol, 1 eq) dissolved in dichloromethane (20 ml) was added and stirring was carried out for 16 h at RT. After monitoring by thin-layer chromatography, the reaction solution was diluted with dichloromethane (250 ml), washed with sat. sodium hydrogen carbonate solution (50 ml), sat. ammonium chloride solution (50 ml), water (50 ml) and sat. NaCl solution (50 ml), dried over sodium sulfate and concentrated under reduced pressure. The crude product was purified by column chromatography (silica gel, 8-10% ethyl acetate in hexane). Yield: 57% (1.6 g, 4.56 mmol).
 

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