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Chemical Structure| 142885-91-4 Chemical Structure| 142885-91-4

Structure of 142885-91-4

Chemical Structure| 142885-91-4

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Product Details of [ 142885-91-4 ]

CAS No. :142885-91-4
Formula : C16H16N4O3S
M.W : 344.39
SMILES Code : COC1=CC=C2N=C(SCC3=NC=C(C)C([N+]([O-])=O)=C3C)NC2=C1
MDL No. :MFCD09840355

Safety of [ 142885-91-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 142885-91-4 ]

* 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 [ 142885-91-4 ]

[ 142885-91-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 142885-91-4 ]
  • [ 73590-85-9 ]
YieldReaction ConditionsOperation in experiment
65g (75%) With sodium methylate; magnesium chloride; potassium carbonate; In methanol; water; ethyl acetate; Example 3 Preparation of 5-methoxy-2-[((4-methoxy-3,5-dimethyl-2-pyridinyl)methyl)-thio)-1H benzimidazole. To a solution of the product from Example 2 (100 g; 0.29 mole) in methanol (500 ml), was added potassium carbonate (138g; 1.0 mole) followed by 30percent sodium methoxide solution (330 ml; 2.0 moles) and anhydrous magnesium chloride (20 g). The contents were refluxed for 2 hours after which the reaction mixture was cooled to ambient temperature, filtered to remove inorganics and concentrated under reduced pressure. To the residue was added water (500 ml) and ethyl acetate (200 ml). The organic layer was separated, dried and chilled to 0.°C and kept overnight to afford 65g (75percent) of the title compound as a crystalline powder.
With hydrogenchloride; sodium methylate; In methanol; water; Example 7 5-Methoxy-2-[(3,5-dimethyl-4-methoxy-2-pyridinyl)methylthio]-1H-benzimidazole (II) 5-Methoxy-2-[(3,5-dimethyl-4-nitro-2-pyridinyl)methylthio]-1H-benzimidazole (IX) (50 gm, 0.145 mole) was dissolved in methanol and heated to 45° C. A solution of sodium methoxide (50 gm, 0.925 mole) in methanol (150 ml) was added dropwise over a period of 3 hours at 45-60° C. Stirring was continued for another 2 hours and then methanol was distilled off under reduced pressure. To the cooled residue was added water (200 ml) followed by concentrated HCl (65 ml) until the pH of the mixture was 7.5. The reaction mixture was extracted with dichloromethane and the dichloromethane layer was washed with water (2*100 ml). The dichloromethane layer was dried over sodium sulfate and concentrated to yield the product as an amber color syrup. Yield was 40.1 gm, about 83.8percent of theoretical. A solid sample was obtained by trituration of the syrup several times with petroleum ether. Melting point was 87-90° C.
  • 2
  • [ 142885-91-4 ]
  • [ 124-41-4 ]
  • [ 73590-85-9 ]
YieldReaction ConditionsOperation in experiment
N-benzyl-N,N,N-triethylammonium chloride; In methanol; at 20℃; for 24h;Heating / reflux; Prepared according to example 9, by substituting CD3ONa-CD3OH with CH3ONa-CH3OH.
 

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