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Chemical Structure| 17821-75-9 Chemical Structure| 17821-75-9

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Chemical Structure| 17821-75-9

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Product Details of [ 17821-75-9 ]

CAS No. :17821-75-9
Formula : C6H3FN2S
M.W : 154.17
SMILES Code : FC1=CC2=NSN=C2C=C1
MDL No. :MFCD00173946
InChI Key :LNZHAYNBUMVVBK-UHFFFAOYSA-N
Pubchem ID :2737263

Safety of [ 17821-75-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 17821-75-9 ]

* 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 [ 17821-75-9 ]

[ 17821-75-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 17821-75-9 ]
  • [ 1347736-74-6 ]
YieldReaction ConditionsOperation in experiment
57% With hydrogen bromide; bromine; In water; for 48h;Reflux; Compound 3 (2.23 g, 14.5 mmol) was charged to a round bottom flask with 30% of 48% hydrobromic acid, and bromine (7.47 mL, 145 mmo) was added dropwise and refluxed for 48 hours. The reaction was cooled to room temperature and diluted with chloroform and deionized water. The bi-phasic mixture is transferred to a separatory funnel, washed several times with water, rinsed with saturated sodium sulfite and rinsed with saturated sodium bicarbonate. The organic layer was extracted, dried over magnesium sulfate, filtered, and concentrated to silica. The compound was purified four times by column chromatography
57% With hydrogen bromide; bromine; for 48h;Reflux; A round-bottom flask was charged with 5-fluorobenzo[c][1,2,5]thiadiazole (2.23 g, 14.5 mmol) followed by 48% hydrobromic acid (30 mL). Molecular bromine (7.47 mL, 145 mmol) was added drop wise and the reaction refluxed for 48 h. The reaction was allowed to cool to room temperature and diluted with chloroform and deionized water. The bi-phasic mixture was transferred to a separatory funnel and washed several times with water, rinsed with saturated sodium sulfite and rinsed with saturated sodium bicarbonate. Organics were collected and dried over magnesium sulfate. The solution was filtered and concentrated with silica. The compound was purified by flash column chromatography using a hexanes/ chloroform gradient isolation of pure fractions afforded a white solid. Yield: 2.58 g (57%). 1H NMR (CDCl3): delta 7.79 (d, 1H, J=8.4 Hz).
44% With hydrogen bromide; bromine; at 120℃; for 48h; To a solution of compound 4 (11.0 g, 71.4 mmol) in 120 mL HBr, bromine (17 mL, 356.8 mmol) was added dropwise slowly at room temperature. After the addition, the reaction mixture was stirred for 48 h at 120 C. After cooling down the mixture to room temperature, the residual bromine was quenched with saturated NaHSO3 solution. The precipitated material was recovered by filtration and then recrystallizied from methylene chloride/ethanol to give 9.8 g (44%) of compound 5. 1H NMR (300 MHz, CDCl3): delta (ppm) 7.81 (d, 1H, J = 8.2 Hz); 13C NMR (75 MHz, CDCl3): delta (ppm) 160.1 (d, 1JC-F = 255.4 Hz), 152.7 (d, 3JC-F = 7.0 Hz), 150.3, 123.9 (d, 2JC-F = 32.4 Hz), 114.0 (d, 3JC-F = 11.5 Hz), 98.2 (d, 2JC-F = 24.3 Hz). HRMS (m/z, EI+) calcd for C6HBr2FN2S 309.8211, found 309.8213.
 

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