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Chemical Structure| 81684-80-2 Chemical Structure| 81684-80-2

Structure of 81684-80-2

Chemical Structure| 81684-80-2

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Product Details of [ 81684-80-2 ]

CAS No. :81684-80-2
Formula : C7H11ClN2
M.W : 158.63
SMILES Code : NC1=CC=CC=C1NC.[H]Cl

Safety of [ 81684-80-2 ]

Application In Synthesis of [ 81684-80-2 ]

* 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 [ 81684-80-2 ]

[ 81684-80-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 81684-80-2 ]
  • [ 152628-03-0 ]
  • [ 152628-02-9 ]
YieldReaction ConditionsOperation in experiment
82% Example 1:Orthophosphoric acid (210 gms) was taken in round bottomed flask and Rho205 (210 gms) was added in portions with vigorous stirring. (Note: Sharp increase in temperature > 200 C). The above mass is allowed to cool to 70 C and 2-n-propyl- 4-methyl-benzimidazole-6-carboxylic acid (70 gms, 0.321 mol) was added slowly. Then N-methylbenzene-l,2-diamine hydrochloride (62.3 gms, 0.321 mol) was added in small portions at same temperature and then the temperature was raised to 125-130 C. After completion, reaction was quenched with ice cold water (1 Lt), adjusted pH of the reaction mixture to 9-10 by the addition of aqueous ammonia solution. Obtained solid was filtered and washed with cold water until the pH of the filtrate becomes neutral. Then the crude solid was washed with hot water until colorless filtrate was observed. The crude solid was boiled in ethyl acetate (700 ml) for 2-3 hrs. The reaction mass was cooled and the suspension was filtered off and dried to yield 2-n-propyl-4-methyl-6-(l-methylbenzimidazol-2-yl)-lH- benzimidazole (V) (80 gms, Yield : 82 %).
EXAMPLE 2; PREPARATION OF 2-n-PROPYL-4-METHYL-6-(1 -METHYL BENZAMIDAZOLE- 2-YL) BENZAMIDAZOLE (FORMULA IV); 7 kg of 2-n-propyl-4-methyl-benzimidazole-6-carboxylic acid, obtained in Example 1 , and 6.2 kg of N-methyl-o-phenylenediamine hydrochloride were charged into a reactor containing 21 kg of polyphosphoric acid (PPA) under stirring. Reaction mass was heated to 150-155 C and maintained at the same temperature for 5-6 hours. Reaction completion was confirmed by thin layer chromatography. Cooled the reaction mass to 90-100 C. 70 L of water was added slowly to the reaction mass at below 100 C and then cooled to 60-70 C. Stirred at same temperature for 45-60 minutes and then cooled to 40-45 C. 140 L of water was added to the reaction mass and pH was adjusted to 5.5-6 with 50% aqueous sodium hydroxide solution. Centrifuged the reaction mass and washed the solid with 35 L of water. Charged the wet cake and 70 L of water into a reactor. Reaction mass was heated to 70-80 C and stirred for 30-45 minutes. Cooled the reaction mass to 40- 45 C, centrifuged the solid and washed the cake with 35 L of water. Repeated the above water slurry process one more time, then dried the material at 70-75 C for 5-6 hours. Charged the dry material into a reactor containing 80 L of tetrahydrofuran under stirring. Heated the mass to reflux and stirred for 10 minutes. Cooled the reaction mass to 5-10 C and stirred for 60-90 minutes. Filtered the solid and washed with 9 L of tetrahydrofuran. Dried the material at 70-75 C under vacuum for 4-5 hours to get 5.9 kg of the title compound.
  • 2
  • [ 81684-80-2 ]
  • [ 152628-03-0 ]
  • [ 884330-09-0 ]
  • [ 884330-18-1 ]
  • [ 884330-17-0 ]
  • [ 152628-02-9 ]
 

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