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[ CAS No. 1443014-87-6 ] {[proInfo.proName]}

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Chemical Structure| 1443014-87-6
Chemical Structure| 1443014-87-6
Structure of 1443014-87-6 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1443014-87-6 ]

CAS No. :1443014-87-6 MDL No. :MFCD28100422
Formula : C7H8BrNO2S2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 282.18 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 1443014-87-6 ]

* 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 [ 1443014-87-6 ]

[ 1443014-87-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 39736-29-3 ]
  • [ 1443014-87-6 ]
YieldReaction ConditionsOperation in experiment
87% With tert.-butylnitrite; copper(ll) bromide; In acetonitrile; at 20℃; General procedure: Twelve millimoles of either anhydrous copper (II) chloride or anhydrous copper (II) bromide were added to a solution of tert-butyl nitrite (15 mmol) in acetonitrile anhydrous (40 mL). The mixture was stirred at 50 C for 1 h, and then 2,5-substituted 4-amino-1,3-thiazole was added slowly. The resulting mixture was stirred at room temperature overnight. The reaction mixture was quenched in water (100 mL). When the precipitate appeared, it was filtered, washed twice with 20 mL of water, and dried under room temperature until a constant weight was reached. The isolated solid was purified by recrystallization in isopropanol. When a viscous mixture appeared, the solution was extracted with ethyl acetate (3 x 25 mL). The organic layers were dried with MgSO4, filtered, and evaporated. The oily solid was then purified by column chromatography on silica gel.
With copper(ll) bromide; isopentyl nitrite; In acetonitrile; at 20℃; General procedure for the synthesis of U2 To a stirred solution of isopentyl nitrite (3.1 mL, 0.023 mmol) in acetonitrile(36.0 mL)was added CuBr2(5.1 g, 0.023 mol) at room temperature and the resulting solution was heated to 50 C . After an hour, the solution was cooled to room temperature and Ul (2.0 g, 9.0 mol) was added slowly. The reaction mixture was further stirred at room temperature for overnight. After reaction completion, the solution was diluted with water (50 mL) and extracted by EtOAc (30 mL x 2). The organic layer was dried over MgS04 and concentrated invacuo. The resulting crude residue was purified by flash column chromatography (-hexane:EtOAc = 10: 1) to give U2.
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