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Chemical Structure| 32873-57-7 Chemical Structure| 32873-57-7

Structure of 32873-57-7

Chemical Structure| 32873-57-7

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Product Details of [ 32873-57-7 ]

CAS No. :32873-57-7
Formula : C4H4ClN3O3S2
M.W : 241.68
SMILES Code : O=S(C1=NN=C(NC(C)=O)S1)(Cl)=O
MDL No. :MFCD00702860
InChI Key :MEJAPGGFIJZHEJ-UHFFFAOYSA-N
Pubchem ID :12894451

Safety of [ 32873-57-7 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314
Precautionary Statements:P260-P280-P303+P361+P353-P301+P330+P331-P304+P340+P310-P305+P351+P338+P310
Class:8
UN#:3261
Packing Group:

Application In Synthesis of [ 32873-57-7 ]

* 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 [ 32873-57-7 ]

[ 32873-57-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 32873-57-7 ]
  • [ 59-66-5 ]
YieldReaction ConditionsOperation in experiment
74% With 1,1,1-triphenylsilylamine; In acetonitrile; for 1.0h;Reflux; Inert atmosphere; General procedure: The sulfonyl chloride (1mmol) is dissolved in 15 ml acetonitrile and then silylamine (1 mmol) is addedslowly. The reaction mixture is refluxed for 1 hour and concentrated withrotary evaporator. If necessary, the product may be further purified by silicagel chromatography (hexane: ethyl acetate).
72% With ammonium hydroxide; In water; for 1.0h;Cooling with ice; The intermediate 2-acetylamino-5-chlorosulfonyl1,3,4-thiadiazole prepared in the present example was gradually added to 60 mL of concentratedAmmonia water, keep the ice bath, plus completed, insulation reaction lh, add 200mL of ice water, ice bath under the acidification of concentrated sulfuric acid to pH 3 ~4, filtered, washed with water and dried at 45 C in air to give 9.1 g of acetazolamide as a white solid in 72% yield (2-amino-5-mercapto-1,3,4-thiadiazole). The purity of the obtained acetazolamide was 99.2%. The product was identified correctly by NMR.
With ammonium hydroxide; at 0 - 10℃; for 1.5h; n 3L three bottles,154.7 g of 2-acetylamino-5-sulfonyl chloride-1,3,4-thiadiazole wet product described above was slowly added in portions600mL ammonia water,The reaction temperature was controlled at 0-10 C for 1.5 hours,After completion of the reaction, add 1L ice water,Stirring and dropping sulfuric acid to pH = 6-7,Filter, the filter cake washed three times,Respectively, 240mL water recrystallization twice,The final product acetazolamide.
  • 2
  • [ 32873-57-7 ]
  • [ 59-66-5 ]
  • bis(5-acetylamino-1,3,4-thiadiazole-2-sulfonyl)amine [ No CAS ]
 

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