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Chemical Structure| 120208-98-2 Chemical Structure| 120208-98-2

Structure of 120208-98-2

Chemical Structure| 120208-98-2

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Product Details of [ 120208-98-2 ]

CAS No. :120208-98-2
Formula : C2H5ClN4O2S2
M.W : 216.67
SMILES Code : O=S(C1=NN=C(N)S1)(N)=O.[H]Cl

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Application In Synthesis of [ 120208-98-2 ]

* 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 [ 120208-98-2 ]

[ 120208-98-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 59-66-5 ]
  • [ 120208-98-2 ]
YieldReaction ConditionsOperation in experiment
96% With hydrogenchloride; In water; for 3.0h;Reflux; [00264] Hydrochloric acid (70 mL, 70.00 mmol, 5.2 equiv) was added to <strong>[59-66-5]acetazolamide</strong> (3 g, 13.34 mmol, 1.0 equiv) and the mixture stirred for 3 hr at reflux. The crude material was purified by column chromatography (CHC13/MeOH: 100/0 to 70/30) to yield the product (2.768 g, 96%)
With hydrogenchloride; water; at 60℃; for 2.0h;Heating / reflux; 22.2 gr of <strong>[59-66-5]acetazolamide</strong>, was dissolved in 100 ml concentrated HC1 solution (35%) and refluxed on A water bath (60 C) for two hours. The SOLVENT WAS EVAPORATED AND THE 5-AMINO-1, 3, 4-THIADIAZOLE-2-SULFBNAMIDE was obtained as a white precipitate. This was dissolved in 50ml of water and neutralized with NAHC03 till pH 7. THE PRODUCT WAS RECRYSTALLIZED from methanol to AFFORD 12G (yield of 54%). White crystals. M. P. 230-231 C.
 

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