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Chemical Structure| 23269-91-2 Chemical Structure| 23269-91-2

Structure of 23269-91-2

Chemical Structure| 23269-91-2

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Product Details of [ 23269-91-2 ]

CAS No. :23269-91-2
Formula : C10H10N2O3S
M.W : 238.26
SMILES Code : SC1=NN=C(C2=CC=C(OC)C(OC)=C2)O1
MDL No. :MFCD01465889

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Application In Synthesis of [ 23269-91-2 ]

* 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 [ 23269-91-2 ]

[ 23269-91-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 75-15-0 ]
  • [ 41764-74-3 ]
  • [ 23269-91-2 ]
YieldReaction ConditionsOperation in experiment
81% With potassium hydroxide; In ethanol; for 8h;Reflux; General procedure: A mixture of (0.01 mol) of the appropriate benzohydrazides 5a-5e, (0.56 g, 0.01 mol) of potassium hydroxide, and(1.14 g, 0.90 cm3, 0.015 mol) of carbon disulfide in 50 cm3 of absolute ethanol was heated under reflux for 8 h. The solvent was evaporated under vacuum. The residue was dissolved in ice-cold water and acidified with dilute hydrochloricacid. The formed precipitate was filtered off, washed with water, dried, and recrystallized from ethanol to give the desired oxadiazole derivatives.
  • 2
  • [ 75-15-0 ]
  • [ 41764-74-3 ]
  • [ 23269-91-2 ]
YieldReaction ConditionsOperation in experiment
60% With potassium hydroxide; In ethanol; for 12h;Reflux; A mixture of 5d (11.90 g, 0.05 mol), potassium hydroxide (3 g, 0.05 mol), carbon disulfide (0.17 mol, 10 mL) in absolute ethanol (50 mL) was heated under reflux with stirring for 12 h. The solvent was evaporated under vacuum. The residue was dissolved in water and acidified with hydrochloric acid (10%). The formed precipitate was filtered, washed with water, dried, and recrystallized from absolute ethanol to give yellowish white solid (7.10 g, 60% yield); mp 237-238 C; IR (KBr, cm-1): 3246 (NH), 1621 (C=N); 1H NMR (DMSO-d6) δ: 8.00 (s, 1H, NH), 7.42 (d, 1H, J = 8.4 Hz, Ar-H), 7.28 (s, 1H, Ar-H), 7.10 (d, 1H, J = 8.4 Hz, Ar-H), 3.80 (s, 6H, 2-OCH3); 13C NMR (DMSO-d6) δ: 177.33, 160.73, 152.27, 149.29, 130.47, 119.88, 114.74, 112.12, 55.80, 55.70.
60% With potassium hydroxide; In ethanol; for 12h;Reflux; General procedure: A mixture of the benzohydrazides 3a-e (0.05 mol), potassium hydroxide(0.05 mol, 2.81 g) and carbon disulfide (0.17 mol, 12.94 g) in50 mL of absolute ethanol was heated at reflux with stirring for 12 h.The solvent was evaporated under vacuum. The resulting solid wasdissolved in water and acidified with 10% HCl. The resulting precipitatewas filtered off, washed with water, dried, and recrystallized fromethanol to generate the corresponding oxadiazole derivatives 4a-e
 

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