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Chemical Structure| 1343453-79-1 Chemical Structure| 1343453-79-1

Structure of 1343453-79-1

Chemical Structure| 1343453-79-1

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Product Details of [ 1343453-79-1 ]

CAS No. :1343453-79-1
Formula : C22H26N2O3
M.W : 366.45
SMILES Code : O=C(C1=CC2=C(NC(C3=CC=CC(N4CCOCC4)=C3)C(C)(C)C2)C=C1)O
MDL No. :MFCD21607267

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Application In Synthesis of [ 1343453-79-1 ]

* 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 [ 1343453-79-1 ]

[ 1343453-79-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1520-70-3 ]
  • [ 1343453-79-1 ]
  • [ 1343458-26-3 ]
YieldReaction ConditionsOperation in experiment
40% Example 98Ethanesulf onic acid [3 ,3 -dimethyl-2- (3 -morpholin-4-yl-phenyl) - 1 ,2,3 ,4-tetrahydro- quinoline-6-carbonyl] -amideTo a suspension of 60percent sodium hydride (745 mg, 18.6 mmol) in N, N-dimethylformamide (2.5 mL) was added <strong>[1520-70-3]ethanesulfonamide</strong> (2.3 g, 19 mmol) at room temperature. The resulting mixture was stirred at 25°C for 1 h. A solution of 3,3-dimethyl-2-(3-morpholin- 4-yl-phenyl)-l,2,3,4-tetrahydro-quinoline-6-carboxylic acid (690 mg, 1.9 mmol) and 1,1'- carbonyldiimidazole (650 mg, 3.8 mmol) in N, N-dimethylformamide (2.0 mL) was stirred at 70°C. After stirring at 70°C for 1 h, the above suspension of <strong>[1520-70-3]ethanesulfonamide</strong> and sodium hydride in N, N-dimethylformamide was added and the mixture was allowed to stir at 25°C for 1 h. Purification by Waters automated flash system (column: Xterra 30 mm x 100 mm, sample manager 2767, pump 2525, detector: ZQ mass and UV 2487, solvent system: acetonitrile and 0.1percent ammonium hydroxide in water) afforded ethanesulfonic acid [3,3-dimethyl-2-(3-morpholin-4-yl-phenyl)-l,2,3,4-tetrahydro-quinoline-6 carbonyl] -amide (347 mg, 40percent) as a white solid: LC/MS m/e calcd for C24H31N3O4S(M+H)+: 458.61, observed: 458.0.
40% To a suspension of 60percent sodium hydride (745 mg, 18.6 mmol) in N,N-dimethylformamide (2.5 mL) was added <strong>[1520-70-3]ethanesulfonamide</strong> (2.3 g, 19 mmol) at room temperature. The resulting mixture was stirred at 25° C. for 1 h. A solution of 3,3-dimethyl-2-(3-morpholin-4-yl-phenyl)-1,2,3,4-tetrahydro-quinoline-6-carboxylic acid (690 mg, 1.9 mmol) and 1,1'-carbonyldiimidazole (650 mg, 3.8 mmol) in N,N-dimethylformamide (2.0 mL) was stirred at 70° C. After stirring at 70° C. for 1 h, the above suspension of <strong>[1520-70-3]ethanesulfonamide</strong> and sodium hydride in N,N-dimethylformamide was added and the mixture was allowed to stir at 25° C. for 1 h. Purification by Waters automated flash system (column: Xterra 30 mm.x.100 mm, sample manager 2767, pump 2525, detector: ZQ mass and UV 2487, solvent system: acetonitrile and 0.1percent ammonium hydroxide in water) afforded ethanesulfonic acid [3,3-dimethyl-2-(3-morpholin-4-yl-phenyl)-1,2,3,4-tetrahydro-quinoline-6-carbonyl]-amide (347 mg, 40percent) as a white solid: LC/MS m/e calcd for C24H31N3O4S (M+H)+: 458.61, observed: 458.0.
 

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