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Chemical Structure| 100460-87-5 Chemical Structure| 100460-87-5

Structure of 100460-87-5

Chemical Structure| 100460-87-5

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Product Details of [ 100460-87-5 ]

CAS No. :100460-87-5
Formula : C14H11FN2O
M.W : 242.25
SMILES Code : O=C1N(CC2=CC=C(F)C=C2)C3=CC=CC=C3N1
MDL No. :MFCD03821190

Safety of [ 100460-87-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 100460-87-5 ]

* 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 [ 100460-87-5 ]

[ 100460-87-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 100460-87-5 ]
  • [ 84946-20-3 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; trichlorophosphate; In water; at 150℃; for 3h; General procedure: To a stirred solution of 1c (1.0 eq.) and POCl3 (10 eq.) was added a few drops of conc. HCl. The reaction mixture was heated to 150 C and stirred for 3 h. After the reaction was completed, the reaction mixture was poured into ice water, neutralized with 1 N aq. NaOH and extracted with ethyl acetate. The organic layer was washed with water, dried over Na2SO4 and concentrated in vacuo to give crude product 1d.
With hydrogenchloride; trichlorophosphate; In water; at 150℃; for 3h; General procedure: To a stirred solution of 1c (1.0 eq.) and POCl3 (10 eq.) was addeda few drops of conc. HCl. The reaction mixture was heated to 150 C and stirred for 3 h. After the reaction was completed, the reaction mixture was poured into ice water, neutralized with 1 N aq. NaOH and extracted with ethyl acetate. The organic layer was washed with water, dried over Na2SO4 and concentrated in vacuo to givecrude product 1d. Alternatively, to a stirred mixture of 2-chlorobenzimidazole (1.0 eq.) and R3CH2Br (1.0 eq.) in dimethylformamide was added N,N-diisopropylethylamine (1.5 eq.). The reaction mixture was heated to 110 C and stirred for 12 h. After the reaction was completed, the reaction mixture was cooled down to room temperature, diluted with ethyl acetate and washed with water. The organic layer was dried over anhydrous MgSO4 and concentrated in vacuo. The crude product was purified by flash column chromatography (ethyl acetate/hexane) to give desired product 1d.
 

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