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Chemical Structure| 1454906-50-3 Chemical Structure| 1454906-50-3

Structure of 1454906-50-3

Chemical Structure| 1454906-50-3

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Product Details of [ 1454906-50-3 ]

CAS No. :1454906-50-3
Formula : C3H2Br2N2S
M.W : 257.93
SMILES Code : BrCC1=NN=C(Br)S1
MDL No. :MFCD27991665

Safety of [ 1454906-50-3 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H314
Precautionary Statements:P280-P305+P351+P338-P310
Class:8
UN#:3261
Packing Group:

Application In Synthesis of [ 1454906-50-3 ]

* 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 [ 1454906-50-3 ]

[ 1454906-50-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 54044-79-0 ]
  • [ 1454906-50-3 ]
YieldReaction ConditionsOperation in experiment
21% With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; at 80℃; for 24h;Inert atmosphere; [000101] To a stirring solution of 2-bromo-5-methyl-l, 3, 4-thiadiazole 57 (2.7 g, 15.08 mmol) in CC (50 mL) under inert atmosphere were added N-bromosuccinimide (2.68 g, 15.08 mmol) and AlphaIotaBetaNu (247 mg, 1.50 mmol) at RT; heated to 80 C and stirred for 24 h. The reaction was monitored by TLC; after completion of the reaction, the reaction mixture was filtered. The filtrate was concentrated in vacuo to obtain the crude. The residue was diluted with water (75 mL) and extracted with EtOAc (2 x 75 mL). The combined organic extracts were dried over sodium sulfate and concentrated in vacuo to the crude. The crude was purified through silica gel flash column chromatography using 5-7% EtOAc/ hexanes to afford compound 58 (800 mg, 21%) as an off-white solid. TLC: 10% EtOAc/ hexanes (Rf. 0.8); NMR (400 MHz, DMSO-rfs): delta 5.14 (s, 2H)
0.150 g With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; at 70℃; for 3h; Step 1 Preparation of 2-bromo-5-(bromomethyl)-1,3,4-thiadiazole To a solution of <strong>[54044-79-0]2-bromo-5-methyl-1,3,4-thiadiazole</strong> (0.50 g, 2.79 mmol) in CCl4 (8 mL) is added N-bromosuccinamide (0.543 g, 3.067 mmol) and azobis-isobutyronitrile (0.022 g, 0.139 mmol) and reaction mixture is heated to 70 C. for 3 hours. Reaction mixture is cooled to 0 C. and the solvent evaporated in vacuo to give the crude material, which is purified by column chromatography eluting in 5% ethylacetate in hexane to afford give the title compound (0.150 g): 1H-NMR (400 MHz, CDCl3) delta 4.75 (s, 2H). LC-MS (m/z): [M+H]=260.8.
  • 2
  • [ 54044-79-0 ]
  • [ 128-08-5 ]
  • [ 1454906-50-3 ]
YieldReaction ConditionsOperation in experiment
With azobisisobutyronitrile; In chloroform; for 4.5h;Reflux; To the mixture of <strong>[54044-79-0]2-bromo-5-methyl-1,3,4-thiadiazole</strong> (3.6 g, 20 mmol) in CC14 (320 ml) was added 1-bromopyrrolidine-2,5-dione (3600 mg, 20 mmol) and (E)-2,2?-(diazene- 1,2-diyl)bis(2-methylpropanenitrile) (190 mg, 1.2 mmol). The resulting mixture was heated at reflux for 4.5 hrs. After filtration through celite and washing of the pad with DCM, the combined filtrate was concentrated and the residue was purified on silica gel column usingEtOAc/hexane as eluting solvents to give 2-bromo-5-(bromomethyl)-1,3,4-thiadiazole. LC/MS:(M+1): 256.83, 258.84, 260.88.
 

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