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Chemical Structure| 90273-31-7 Chemical Structure| 90273-31-7

Structure of 90273-31-7

Chemical Structure| 90273-31-7

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Product Details of [ 90273-31-7 ]

CAS No. :90273-31-7
Formula : C9H7ClO2S2
M.W : 246.73
SMILES Code : O=S(C1=C(C)SC2=CC=CC=C12)(Cl)=O
MDL No. :MFCD19200125

Safety of [ 90273-31-7 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H311-H314-H331
Precautionary Statements:P260-P264-P270-P271-P280-P301+P330+P331-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P310-P403+P233-P405-P501
Class:6.1(8)
UN#:2928
Packing Group:

Application In Synthesis of [ 90273-31-7 ]

* 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 [ 90273-31-7 ]

[ 90273-31-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 90273-31-7 ]
  • [ 33084-49-0 ]
  • N-(4-bromo-3-methyl-5-isoxazolyl)-2-methylbenzo[b]thiophene-3-sulfonamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
With NaH; In tetrahydrofuran; water; EXAMPLE 41 N-(4-Bromo-3-methyl-5-isoxazolyl)-2-methylbenzo[b]thiophene-3-sulfonamide NaH (60% oil dispersion, 2.5 mmoles, 100 mg) was added to a solution of <strong>[33084-49-0]4-bromo-3-methyl-5-aminoisoxazole</strong> (1.0 mmoles, 0.177 g). THF (5 ml) at 0 C. was added, and the resulting reaction mixture was stirred 10 min at 0 C. 2-Methylbenzo[b]thiophene-3-sulfonyl chloride (1.2 mmoles, 0.28 g) was added, and the reaction mixture was stirred for 20 min at 0 C., then warmed to ambient temperature for 1 hr followed by addition of 2 ml of water. The mixture was diluted with ethyl acetate (100 ml) and washed with 2% HCl (2*50 ml), then brine (50 ml). The organic phase was dried (MgSO4), filtered and concentrated. Recrystallization of the crude reaction mixture resulted in 0.24 g (63%) of N-(4-bromo-3-methyl-5-isoxazolyl)-2-methylbenzo[b]thiophene-3-sulfonamide as an off-white solid, m.p. 131-133 C.
With NaH; In tetrahydrofuran; water; EXAMPLE 41 N-(4-Bromo-3-methyl-5-isoxazolyl)-2-methylbenzo[b]thiophene-3-sulfonamide NaH (60% oil dispersion, 2.5 mmoles, 100 mg) was added to a solution of <strong>[33084-49-0]4-bromo-3-methyl-5-aminoisoxazole</strong> (1.0 mmoles, 0.177 g). THF (5 ml) at 0 C. was added, and the resulting reaction mixture was stirred 10 min at 0 C. 2-Methylbenzo[b]thiophene-3-sulfonyl chloride (1.2 mmoles, 0.28 g) was added, and the reaction mixture was stirred for 20 min at 0 C., then warmed to ambient temperature for 1 hr followed by addition of 2 ml of water. The mixture was diluted with ethyl acetate (100 ml) and washed with 2% HCl (2*50 ml), then brine (50 ml). The organic phase was dried (MgSO4), filtered and concentrated. Recrystallization of the crude reaction mixture resulted in 0.24 g (63%) of N-(4-bromo-3-methyl-5-isoxazolyl)-2-methylbenzo[b]thiophene-3-sulfonamide as an off-white solid, m.p. 131-133 C.
 

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