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Chemical Structure| 597545-16-9 Chemical Structure| 597545-16-9

Structure of 597545-16-9

Chemical Structure| 597545-16-9

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Product Details of [ 597545-16-9 ]

CAS No. :597545-16-9
Formula : C8H6BrNOS
M.W : 244.11
SMILES Code : COC1=CC=C(Br)C=C1N=C=S
MDL No. :MFCD03923610

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Application In Synthesis of [ 597545-16-9 ]

* 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 [ 597545-16-9 ]

[ 597545-16-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 463-71-8 ]
  • [ 6358-77-6 ]
  • [ 597545-16-9 ]
YieldReaction ConditionsOperation in experiment
With sodium carbonate; In acetone; at 0 - 20℃; for 2.5h; A solution of 2 (1 eq) and sodium carbonate (1.5 eq) in acetone was stirred under an atmosphere of nitrogen in an ice bath. Thiophosgene (1.5 eq) was added drop wise over 30 minutes. The reaction was stirred for another 30 minutes in the ice bath before being removed and allowed to warm to RT. The reaction was stirred at RT for 1.5 h and then the reaction solution was concentrated under vacuum. Toluene was added to the crude product and removed under vacuum to azetrope off any residual thiophosgene and afford the product 3. MS: MH+=244
With sodium hydrogencarbonate; In chloroform; water; at 20℃; for 1h; Intermediate 20: Step a 4-Bromo-2-isothiocyanato-1-methoxy-benzene A solution of sodium bicarbonate (3.74 g, 44.5 mmol) in water (75 mL) was added to commercially available 5-bromo-2-methoxy-phenylamine (3 g, 14.8 mmol) in chloroform (75 mL). Thiophosgene (1.42 mL, 18.6 mmol) was then added. The biphasic solution was stirred at room temperature for 1 h. The phases were separated and the aqueous phase was extracted with CH2Cl2. The organic phase was dried (Na2SO4), filtered, and concentrated, yielding the crude title compound as an off-white solid.
With sodium hydrogencarbonate; In chloroform; water; at 20℃; for 1h; A solution of sodium bicarbonate (3.74 g, 44.5 mmol) in water (75 mL) was added to commercially available 5-bromo-2-methoxy-phenylamine (3 g, 14.8 mmol) in chloroform (75 mL). Thiophosgene (1.42 mL, 18.6 mmol) was then added. The biphasic solution was stirred at room temperature for 1 h. The phases were separated and the aqueous phase was extracted with CH2Cl2. The organic phase was dried (Na2SO4), filtered, and concentrated, yielding the crude title compound as an off-white solid.
With sodium hydrogencarbonate; In chloroform; water; Intermediate 14: step a 4-Bromo-2-isothiocyanato-1-methoxy-benzene A solution of sodium bicarbonate (3.74 g, 44.5 mmol) in water (75 mL) was added to commercially available 5-bromo-2-methoxy-phenylamine (3 g, 14.8 mmol) in chloroform (75 mL). Thiophosgene (1.42 mL, 18.6 mmol) was then added. The biphasic solution was stirred at room temperature for 1 h. The phases were separated and the aqueous phase was extracted with CH2Cl2. The organic phase was dried (Na2SO4), filtered, and concentrated, yielding the crude title compound as an off-white solid.

 

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