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Chemical Structure| 3653-05-2 Chemical Structure| 3653-05-2

Structure of 3653-05-2

Chemical Structure| 3653-05-2

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Product Details of [ 3653-05-2 ]

CAS No. :3653-05-2
Formula : C15H15IN2
M.W : 350.20
SMILES Code : C[N+]1=C(C2=CC=CC=C2)N(C)C3=CC=CC=C31.[I-]

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Application In Synthesis of [ 3653-05-2 ]

* 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 [ 3653-05-2 ]

[ 3653-05-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2622-63-1 ]
  • [ 74-88-4 ]
  • [ 3653-05-2 ]
YieldReaction ConditionsOperation in experiment
95% In N,N-dimethyl-formamide; for 0.0833333h;Microwave irradiation; General procedure: 2 mmols of 1-methyl-2-aryllbenzimidazole was placed ina 100 mL round bottom flask. After adding 2 mL of DMF into the flask, 3 mmols of alkylhalide was added onto the mixture dropwise under stirring. Attaching with a reflux condenser, the reaction system was placed in the CEM-Mars6 multimode microwave synthesis system and exposed to 120 W microwaves. The progress and termination of the reaction was monitored by TLC with a mixture of methanol and chloroform (1:9) as the eluent. After termination of the reaction, the heterogenous mixture obtained was cooled to room temperature and then poured into diethyl ether (30mL). The precipitate was collected by filtration. Diethylether threatment was repeated two times in order to remove solvent residue. The insoluble light brown/beige solids obtained by filtration was allowed to crystallize in water. Compounds 8-28 were synthesised from appropriate 1-methl-2-arylbenzimidazole derivatives and alkyl halides using the same procedure.
91% In dichloromethane; at 30℃; for 17h; Methylene chloride (20 mL) was added to 7 (3.00 g, 14.4 mmol) in a 50 mL round-bottom flask and stirred until fully dissolved. Iodomethane (2.7 mL, 43.4 mmol) was added and the mixture was stirred at 30 °C closed for 17 h. The solvent was evaporated at 45 °C using dynamic vacuum and diethyl ether was added. The solid was collected by vacuum filtration, washed with diethyl ether, and dried under vacuum at 40 °C, yielding HB (4.59 g, 91percent) as an off-white powder. 1H NMR (500 MHz, DMSO-d6, delta 8.15 (dd, J= 6.2, 3.1 Hz, 2H), 7.93 (d, J= 7.0 Hz, 2H), 7.88-7.73 (m, 5H), 3.91 (s, 6H). 13C NMR (125 MHz, DMSO-d6, delta: 150.29, 132.91, 131.68, 130.76, 129.42, 126.61,120.96, 113.39, 32.85. ESI-MS m/z calcd for C15H15N2+ [M+]: 223.123, found 223.124.
 

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