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Chemical Structure| 1403865-40-6 Chemical Structure| 1403865-40-6

Structure of 1403865-40-6

Chemical Structure| 1403865-40-6

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Product Details of [ 1403865-40-6 ]

CAS No. :1403865-40-6
Formula : C11H19NO2
M.W : 197.27
SMILES Code : O=C(OC(C)(C)C)NC1(C2)CC2(C)C1
MDL No. :MFCD30802634

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Application In Synthesis of [ 1403865-40-6 ]

* 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 [ 1403865-40-6 ]

[ 1403865-40-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 65862-01-3 ]
  • [ 75-65-0 ]
  • [ 1403865-40-6 ]
YieldReaction ConditionsOperation in experiment
66% With diphenyl phosphoryl azide; triethylamine; at 30℃;Molecular sieve; [0186] 5-2 (0.500 g, 3.96 mmol) was dissolved in tert-BuOH (19.8 mL). EtiN (0.802 g, 7.93 mmol, 1 .1 5 mL) and activated 3 A molecular sieves were added followed by diphenylphosphoryl azide (1.025 mL, 4.76 mmol). The resulting solution was stirred at 30 C for 4 h, and then heated to reflux overnight. The solution was cooled to rt and then concentrated under reduced pressure. The residual oil was diluted with EtOAc (20 mL) and H2O (20 mL), and extracted with EtOAc (4 x 20 mL). The combined organics were dried (NaiSCM) and concentrated to afford the crude product that was further purified by flash chromatography (81O2, Hexanes/EtOAc) to provide 5-3 (0.513 g, 66%) as a semi-pure white solid. ' 1NMR (400 MHz, CDCI.3) δ 4.87 (br s, N/7. 1 H), 1.85 (s, 6 H), 1.43 (s, 9 H), 1 .21 (s, 3 H); LC/MS (APCI) m/z 98.1 j ( 1 i i Ι ΝΧ '- ΠΟ1H I .
35.7% With diphenyl phosphoryl azide; triethylamine; at 20℃; for 28h;Reflux; Diphenylphosphonic azide (0.340 mL, 1.577 mmol) was added dropwise to a solution of 3-methylbicyclo[l . l .l]pentane-l-carboxylic acid (0.199 g, 1.577 mmol) and TEA(0.220 mL, 1.577 mmol) in dry tert-butanol (6 mL). The solution was stirred at room temperature for 4 h and then heated to reflux for 24 h. The solvent was evaporated under reduced pressure and the residue was extracted three times with tert-butyl methyl ether. The combined organic phase was washed with saturated aqueous sodium bicarconate solution and dried over anhydrous magnesium sulfate. After filtration and evaporation of the solvent under reduced pressure the residue was purified by column chromatography (0-5% ethyl acetate in hexanes) to afford tert-butyl 3-methylbicyclo[l .l . l]pentan-l- ylcarbamate (0.111 g, 0.563 mmol, 35.7 % yield); 1H NMR (400 MHz, DMSO-d6) δ ppm 1.74 (s, 6 H), 1.36 (s, 9 H), 1.17 (s, 3 H).
 

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