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Chemical Structure| 98827-44-2 Chemical Structure| 98827-44-2

Structure of 98827-44-2

Chemical Structure| 98827-44-2

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Product Details of [ 98827-44-2 ]

CAS No. :98827-44-2
Formula : C8H7NO5S2
M.W : 261.28
SMILES Code : COC(=O)C1=C(O)C2=C(C=CS2)S(=O)(=O)N1
MDL No. :MFCD08460399
InChI Key :QHDGDSKIUCBIGS-UHFFFAOYSA-N
Pubchem ID :54707628

Safety of [ 98827-44-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P261-P280-P305+P351+P338

Application In Synthesis of [ 98827-44-2 ]

* 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 [ 98827-44-2 ]

[ 98827-44-2 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 106820-63-7 ]
  • [ 98827-44-2 ]
YieldReaction ConditionsOperation in experiment
79% With sodium methylate; In methanol; for 2.0h;Reflux; 8.5 g of TNXK-1, 27% sodium methoxide 27.2 g and anhydrous methanol 15 ml stirring to reflux 2 hours, cooling, water 200 ml dilution, use 10% hydrochloric acid to neutral, evaporate the solvent, and then cooling the residue 10% hydrochloric acid to the PH is 3. Filtering, the filter cake is then washing with water, drying, be 5.6 g yellow-green solid TNXK-2, yield 79%.
With water; sodium methylate; In methanol; at 75.0℃; for 25.0h; 2) Weigh 10g of crude product II (34mmol) and 32g of 27% sodium methoxide (160mmol) in 18ml of anhydrous methanol, heat to 75C under stirring and reflux for 25h, cool, add 200ml of water and dilute with 10% The hydrochloric acid was adjusted to neutrality, the solvent was distilled off, the remaining cooling material was adjusted to pH 3 with 10% hydrochloric acid, filtered, the filter cake was washed with water 3 times and dried to obtain a yellow solid crude product II' (4.92 g, 76.5%).
  • 3
  • [ 98827-44-2 ]
  • [ 59804-37-4 ]
  • 4
  • [ 504-29-0 ]
  • [ 98827-44-2 ]
  • [ 616-38-6 ]
  • [ 59804-37-4 ]
YieldReaction ConditionsOperation in experiment
83% 260 kg of 4-hydroxy-2H-thieno [2,3-e] -1,2-thiazine-3-carboxylic acid methyl ester 1,1-dioxide were dissolved in500kgDMF, add potassium carbonate 150kg, warmed to 140 C, and dropping 120kg of dimethyl carbonate, 2h drop end, after the dropwise addition, the reaction was continued for 5h, then add 140kg of potassium carbonate, dropping 300 kg of 2 - aminopyridine in dimethylformamide (DMF) (120kg 2-aminopyridine dissolved in 180 kg DMF), 2h addition was complete, the reaction was continued for 5h. After the reaction, cooling and filtering to remove potassium carbonate, the filtrate was recovered under reduced pressure most of the DMF, the residue was added mass concentration of 3% sodium hydroxide alkaline water, activated carbon bleaching, filtration, the filtrate was purified hydrochloric acid to pH = 3 -4, precipitated yellowish solid, centrifuged, the material was washed until neutral, dried, to give a yellow solid 276kg, yield 83%, product purity 99.85%.
  • 5
  • [ 98827-44-2 ]
  • [ 77-78-1 ]
  • [ 59804-25-0 ]
YieldReaction ConditionsOperation in experiment
86% With sodium hydroxide; In methanol; at 20.0℃; for 3.0h; 5.3 g of TNXK-3 and 20 ml of methanol were added to a reaction flask. Stir at room temperature. Separately add dimethyl sulfate 3.7 g methanol (5 ml) solution and 50% sodium hydroxide solution (5 ml). After the completion of the dropping, room temperature reaction 3 hours, cooling to 10 degrees, the water 50 ml dilution, use 10% hydrochloric acid to the PH is 3. Filtering, the filter cake after the water washing, drying, recrystallization with methanol, 60 degrees decompression drying, getting white solid 4.8 g, yield 86%.
3.6 g With sodium hydroxide; In methanol; at 20.0℃; for 3.5h; 3) Weigh 4g of crude product II'(15.3mmol) and dissolve it in 20ml of methanol, add dropwise 2.8g of dimethyl sulfate (21.9mmol) in methanol (5ml) and 50% sodium hydroxide solution ( 4ml). After the dripping is completed, react for 3.5h at room temperature, then cool to 10C, add 40ml of water to dilute and adjust the pH to 3 with 10% hydrochloric acid. After suction filtration, the filter cake was washed with water 3 times and dried, and then recrystallized with methanol, and dried under reduced pressure at 60 C. to obtain an off-white solid ester compound II (3.6 g, 78.7%) containing a thiazine ring.
 

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