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Chemical Structure| 368890-20-4 Chemical Structure| 368890-20-4

Structure of 368890-20-4

Chemical Structure| 368890-20-4

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Product Details of [ 368890-20-4 ]

CAS No. :368890-20-4
Formula : C15H12ClF2N3O2S
M.W : 371.79
SMILES Code : FC(F)OC1=CC=C2NC(SCC3=NC=CC(Cl)=C3OC)=NC2=C1
MDL No. :MFCD07368270

Safety of [ 368890-20-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H317-H319
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 368890-20-4 ]

* 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 [ 368890-20-4 ]

[ 368890-20-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 503058-51-3 ]
  • [ 97963-62-7 ]
  • [ 368890-20-4 ]
YieldReaction ConditionsOperation in experiment
92% With sodium hydroxide; In water; toluene; at 55 - 65℃; for 4 - 6h; At 55-65 0C, a solution of 4-chloro-2-chloromethyl-3-methoxypyridinium chloride (10.0 kg, 43.8 mol) in water (20 L) was added over 2-3 h to a mixture of 5-difluoromethoxy-1 H-benzimidazole-2-thiol (8.84 kg, 40.9 mol), toluene (43 L), water (21 L) and 40% aqueous NaOH (10.3 kg, 103 mol). Stirring at 60 0C was continued for 2-3 h before the reaction mixture was cooled to 10-15 0C. The precipitate was centrifuged off, washed with toluene (16 L) and re-pulped in water (122 L). Centrifugation followed by an aqueous rinse (32 L) and drying at 35 0C in vacuo gave 5-difluoromethoxy-2-[(4-chloro-3-methoxy- 2-pyridinyl)methylthio]-1 H-benzimidazole mono hydrate (KF = 4.6%) as an off-white solid (m. p. 95-99 0C); yield 14.2 kg (92%). EPO <DP n="18"/>- -1H-NMR (200 MHz, DMSO-d6): delta= 3.55 (br s, NH + H2O), 3.92 (s, 3H), 4.79 (s, 2H), 6.97 (dd, 8.6 Hz, 2.3 Hz, 1 H), 7.16 (t, 74.8 Hz, 1 H), 7.28 (d, 2.2 Hz, 1 H), 7.47 (d, 8.7 Hz, 1 H), 7.55 (d, 5.3 Hz, 1 H), 8.25 (d, 5.2 Hz, 1 H); LC-MS: MH+ = 372/374.
  • 2
  • [ 409098-85-7 ]
  • [ 97963-62-7 ]
  • [ 368890-20-4 ]
YieldReaction ConditionsOperation in experiment
82.8% Example 2: Synthesis of (5-difluoromethoxy)-2-[(4-chloro-3-methoxy-2-pyridinyl)methyl]thio-1H-benzimidazole (IV) The suspension, containing 2-chloromethyl-3-methoxy-4-chloropyridine, obtained according to the procedure of example 1, is diluted at about 15-25C with 219 ml of methanol until complete dissolution. 58 g (0.319 mol) of NaOCH3 (30% w/w solution) are dropped into the solution, keeping the inner temperature below 25C, finally washing with 10 ml of methanol. The mixture is kept at approx. 15-25C for 1 hour, then 76 g (0.351 mol) of 5-difluoromethoxy-2-mercapto-benzimidazole are added, stirring for 30 minutes. 63 g (0.351 mol) of NaOCH3 (30% w/w solution) are then added dropwise, keeping the inner temperature at approx. 20-35C. After completion of the addition the mixture is washed with 10 ml of methanol. The resulting suspension is kept for about 1 hour at about 15-25C. After completion of the reaction, a solution of 197 ml of water and 19 ml (0.191 mol) of 30% NaOH is added dropwise, thereby obtaining a suspension which is kept under stirring for approx. 30 minutes and concentrated by distillation of 410 ml of solvent, reaching 87C inner temperature. Thereafter, 131 ml of water are added dropwise, followed by 119 ml of toluene at a temperature below 80C. The mixture is refluxed for 30 minutes to obtain a solution from which the product crystallizes upon slow cooling. Alternatively, the organic phase is separated and subjected to the subsequent step. When carrying out the crystallization of intermediate (IV), this is recovered by filtration, after cooling at about 15-25 for 1 hour, and washed twice on the filter first with 120 ml of toluene, then with water, until neutral pH and absence of chlorides. 155 g of wet product are obtained, which is dried under vacuum to obtain 98.1 g of dry product (yield = 82.8%).
82.8% The suspension, containing 2-chloromethyl-3-methoxy-4-chloro-pyridine, obtained according to the procedure of example 1, is diluted at about 15-25 C. with 219 ml of methanol until complete dissolution. 58 g (0.319 mol) of NaOCH3 (30% w/w solution) are dropped into the solution, keeping the inner temperature below 25 C., finally washing with 10 ml of methanol. The mixture is kept at approx. 15-25 C. for 1 hour, then 76 g (0.351 mol) of 5-difluoromethoxy-2-mercapto-benzimidazole are added, stirring for 30 minutes. 63 g (0.351 mol) of NaOCH3 (30% w/w solution) are then added dropwise, keeping the inner temperature at approx. 20-35 C. After completion of the addition the mixture is washed with 10 ml of methanol. The resulting suspension is kept for about 1 hour at about 15-25 C. After completion of the reaction, a solution of 197 ml of water and 19 ml (0.191 mol) of 30% NaOH is added dropwise, thereby obtaining a suspension which is kept under stirring for approx. 30 minutes and concentrated by distillation of 410 ml of solvent, reaching 87 C. inner temperature. Thereafter, 131 ml of water are added dropwise, followed by 119 ml of toluene at a temperature below 80 C.
 

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