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Chemical Structure| 155778-36-2 Chemical Structure| 155778-36-2

Structure of 155778-36-2

Chemical Structure| 155778-36-2

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Product Details of [ 155778-36-2 ]

CAS No. :155778-36-2
Formula : C7H9N3OS
M.W : 183.23
SMILES Code : O=C1NCCCC2=C1SC(N)=N2
MDL No. :MFCD00460522

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Application In Synthesis of [ 155778-36-2 ]

* 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 [ 155778-36-2 ]

[ 155778-36-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 17583-10-7 ]
  • [ 155778-36-2 ]
YieldReaction ConditionsOperation in experiment
83% With sodium azide; sulfuric acid; In chloroform; at 20℃; for 50h; To a stirred solution of <strong>[17583-10-7]2-amino-5,6-dihydro-4H-benzothiazol-7-one</strong> (10 g, 59 mmol) in chloroform (250 mL) was added concentrated H2S04 at room temperature. Sodium azide (7.6 g, 117 mmol) was then carefully added to the mixture over two hours (vigorous gas evolution). The reaction mixture was further stirred at room temperature for 48 hours. The mixture was poured into crushed ice and a saturated solution of NaHCC"3 was added until the pH of the solution was about 9. The formed precipitate was filtered off and washed with H20 and AcOEt. The solid was dried in the oven (T = 50°C) to yield 9 g (83percent) of intermediate 5 that was used in the next step without further purification.
With sodium azide; sulfuric acid; In chloroform; at 20℃; for 50h; To a stirred solution of <strong>[17583-10-7]2-amino-5,6-dihydro-4H-benzothiazol-7-one</strong> (10 g, 59 mmol) in chloroform (250 mL) was added concentrated H2SO4 at room temperature. Sodium azide (7.6 g, 117 mmol) was then carefully added to the mixture over two hours (vigorous gas evolution). The reaction mixture was further stirred at room temperature for 48 hours. The mixture was poured into crushed ice and a saturated solution of NaHCO3 was added until the pH of the solution was about 9. The formed precipitate was filtered off and washed with H2O and AcOEt. The solid was dried in the oven (T=50° C.) to yield 9 g (83percent) of intermediate 5 that was used in the next step without further purification.
 

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