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Chemical Structure| 1142-18-3 Chemical Structure| 1142-18-3

Structure of 1142-18-3

Chemical Structure| 1142-18-3

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Product Details of [ 1142-18-3 ]

CAS No. :1142-18-3
Formula : C14H15NO
M.W : 213.28
SMILES Code : CNC1=CC=C(OCC2=CC=CC=C2)C=C1
MDL No. :MFCD00658358

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Application In Synthesis of [ 1142-18-3 ]

* 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 [ 1142-18-3 ]

[ 1142-18-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1142-18-3 ]
  • [ 89776-57-8 ]
  • N-[4-(benzyloxy)phenyl]-N,1,2-trimethyl-1H-pyrrole-3-carboxamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
Step A: N-(4-Benzyloxyphenyl)-N,1,2-trimethyl-pyrrole-3-carboxamide To a suspension of <strong>[89776-57-8]1,2-dimethylpyrrole-3-carboxylic acid</strong> (2.085 g; 15 mmol) in 1,2-dichloroethane (40 mL) there is added 1-chloro-N,N,2-trimethyl-prop-1-en-1-amine (2.37 mL; 17.9 mmol), and the solution formed is stirred for 1 hour. To the resulting solution there is added, dropwise, an ice-cold solution of 4-benzyloxy-N-methyl-aniline (3.73 g; 15 mmol) and N-ethyl-N-isopropyl-propan-2-amine (7.75 mL; 45 mmol) in 1,2-dichloroethane (40 mL). The reaction mixture is stirred at ambient temperature for 1 hour; it is then diluted with dichloromethane (250 mL) and washed with water (2*30 mL), dried over Na2SO4 and evaporated. The crude product is triturated with diethyl ether and the solid formed is filtered off to yield the title compound. IR: nu: >C=O: 1616 cm-1; amide: 1508 cm-1; C-O-C: 1230, 1172, 1009 cm-1
Step C: N-[4-(Benzyloxyfrl,enylJ-N,1,2-trirnethyl-1H-pyrrote-3-carboxan,jdeThe acid obtained from Step B (1 g, 7.19 mmol) is dissolved in dichloromethane (20 ml) and to this is added l-chloro-N,N,2-trimethyl-l-propenylamine (1.15 g, 8.62 mrnol) and stirred at ambient temperature for 2 hours, The mixture is concentrated to an oil which is re-dissolved in toluene (50 mL). A solution of 4-(benzyloxy)-N-methylaniline (1.84 g, 8.62 mmol) in toluene (10 ml) is added and the resultant mixture is stirred at reflux for 2 hours.The reaction is allowed to cool to ambient temperature and lefi to stand for cci 16 h. The reaction is partitioned between ethyl acetate and water, separated, and the organics are washed with water, dried over magnesium sulphate, filtered and concentrated. The crude product is purified on CombiFlash (80 g silica, Hex to 60% EtOAe) to obtain the desired product as a solid.LC/MS (C21H22N202) 335 [M+H] RT 1.33 (Method B)
 

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