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Chemical Structure| 90359-73-2 Chemical Structure| 90359-73-2

Structure of 90359-73-2

Chemical Structure| 90359-73-2

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Product Details of [ 90359-73-2 ]

CAS No. :90359-73-2
Formula : C13H19NO2
M.W : 221.30
SMILES Code : O=C(N(CC)CC)C1=CC=C(OC)C=C1C

Safety of [ 90359-73-2 ]

Application In Synthesis of [ 90359-73-2 ]

* 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 [ 90359-73-2 ]

[ 90359-73-2 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 90359-73-2 ]
  • [ 102151-33-7 ]
  • [ 1409950-48-6 ]
  • 2
  • [ 90359-73-2 ]
  • [ 102151-33-7 ]
  • [ 1409950-49-7 ]
YieldReaction ConditionsOperation in experiment
84% With tert.-butyl lithium; In tetrahydrofuran; pentane; Step 1 To a solution of N,N-diethyl-4-methoxy-2-methylbenzamide (1 g, 4.52 mmol) in THF (9 ml) at -78 C. was added dropwise tert-butyllithium 1.7 M in pentane (3.19 ml, 5.42 mmol) and the solution was stirred for 0.5 h before addition of <strong>[102151-33-7]3-chloro-4-methoxybenzonitrile</strong> (0.757 g, 4.52 mmol) in THF (9 ml). The resulting solution was warmed to rt and stirred for 16 h. The reaction mixture was quenched with water, neutralized with 1 N HCl. The precipitated solid was collected and washed with water to give 3-(3-chloro-4-methoxyphenyl)-6-methoxyisoquinolin-1-ol (1.2 g, 84% yield) as a solid after drying. MS: MS m/z 316.1 (M++1).
84% To a solution of N,N-diethyl-4-methoxy-2-methylbenzamide (1 g, 4.52 mmol) in THF (9 ml) at -78 C. was added dropwise tert-butyllithium 1.7 M in pentane (3.19 ml, 5.42 mmol) and the solution was stirred for 0.5 h before addition of <strong>[102151-33-7]3-chloro-4-methoxybenzonitrile</strong> (0.757 g, 4.52 mmol) in THF (9 ml). The resulting solution was warmed to rt and stirred for 16 h. The reaction mixture was quenched with water, neutralized with 1 N HCl. The precipitated solid was collected and washed with water to give 3-(3-chloro-4-methoxyphenyl)-6-methoxyisoquinolin-1-ol (1.2 g, 84% yield) as a solid after drying. MS: MS m/z 316.1 (M++1)
  • 3
  • [ 331-62-4 ]
  • [ 90359-73-2 ]
  • [ 1409950-50-0 ]
  • 4
  • [ 331-62-4 ]
  • [ 90359-73-2 ]
  • [ 1409950-51-1 ]
YieldReaction ConditionsOperation in experiment
69% With tert.-butyl lithium; In tetrahydrofuran; pentane; Step 1 To a solution of N,N-diethyl-4-methoxy-2-methylbenzamide (1.00 g, 4.52 mmol) in THF (9 ml) at -78° C. was added dropwise tert-butyllithium 1.7 M in pentane (3.19 ml, 5.42 mmol) and the solution was stirred for 0.5 h before addition of <strong>[331-62-4]3-fluoro-4-methoxybenzonitrile</strong> (0.683 g, 4.52 mmol) in THF (9 ml). The resulting solution was warmed to rt and stirred for 16 h. The reaction mixture was quenched with water, neutralized with 1 N HCl. The precipitated solid was collected and washed with water to give 3-(3-fluoro-4-methoxyphenyl)-6-methoxyisoquinolin-1-ol (926 mg, 69percent yield) as a solid after drying. MS: MS m/z 300.1 (M++1).
69% To a solution of N,N-diethyl-4-methoxy-2-methylbenzamide (1.00 g, 4.52 mmol) in THF (9 ml) at ?78° C. was added dropwise tert-butyllithium 1.7 M in pentane (3.19 ml, 5.42 mmol) and the solution was stirred for 0.5 h before addition of <strong>[331-62-4]3-fluoro-4-methoxybenzonitrile</strong> (0.683 g, 4.52 mmol) in THF (9 ml). The resulting solution was warmed to rt and stirred for 16 h. The reaction mixture was quenched with water, neutralized with 1 N HCl. The precipitated solid was collected and washed with water to give 3-(3-fluoro-4-methoxyphenyl)-6-methoxyisoquinolin-1-ol (926 mg, 69percent yield) as a solid after drying. MS: MS m/z 300.1 (M++1)
 

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