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Chemical Structure| 154594-16-8 Chemical Structure| 154594-16-8

Structure of 154594-16-8

Chemical Structure| 154594-16-8

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Product Details of [ 154594-16-8 ]

CAS No. :154594-16-8
Formula : C8H9N5
M.W : 175.19
SMILES Code : NNC1=CC=C(N2C=NN=C2)C=C1
MDL No. :MFCD02663159

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Application In Synthesis of [ 154594-16-8 ]

* 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 [ 154594-16-8 ]

[ 154594-16-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 29882-07-3 ]
  • [ 154594-16-8 ]
  • 2-[5-(1,2,4-triazol-4-yl)-1H-indol-3-yl]ethylamine [ No CAS ]
YieldReaction ConditionsOperation in experiment
49% With ammonia;hydrogenchloride; In methanol; ethanol; dichloromethane; water; 1. N-(1-Benzylpiperidin-4-yl)-N-[2-(5-(1,2,4-triazol-4-yl)-1H-indol-3-yl)ethyl]amine Hydrogen Oxalate 4-(1,2,4-Triazol-4-yl)phenylhydrazine (3 g, 17.12 mmol) and <strong>[29882-07-3]4-chlorobutyraldehyde dimethyl acetal</strong> (2.35 g, 15.41 mmol) were heated at reflux in ethanol/water (5:1, 120 ml) in the presence of concentrated hydrochloric acid (3.77 ml) under nitrogen for 6 hours. The volatiles were evaporated and the residue partitioned between 2M sodium hydroxide (50 ml) and n-butanol. The organic layer was separated and the solvent evaporated. The crude product was purified by column chromatography on silica using dichloromethane/methanol/ammonia (40:8:1) to give 2-[5-(1,2,4-triazol-4-yl)-1H-indol-3-yl]ethylamine as a brown oil (1.9 g, 49percent).
 

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