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Chemical Structure| 944401-72-3 Chemical Structure| 944401-72-3

Structure of 944401-72-3

Chemical Structure| 944401-72-3

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Product Details of [ 944401-72-3 ]

CAS No. :944401-72-3
Formula : C6H4BrN3
M.W : 198.02
SMILES Code : NC1=NC=C(Br)C(=C1)C#N
MDL No. :MFCD09907918
InChI Key :WEMPYBBWDHFMFG-UHFFFAOYSA-N
Pubchem ID :53440577

Safety of [ 944401-72-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 944401-72-3 ]

* 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 [ 944401-72-3 ]

[ 944401-72-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 42182-27-4 ]
  • [ 944401-72-3 ]
YieldReaction ConditionsOperation in experiment
78% With N-Bromosuccinimide; In N,N-dimethyl-formamide; at -18℃; for 1h; Step 2.1 : 2-Amino-5-bromo-isonicotinonitrile.A solution of <strong>[42182-27-4]2-amino-isonicotinonitrile</strong> (10.0 g, 83.9 mmol) in DMF (20 mL) was cooled to -18°C (ice / MeOH bath), treated with NBS (16.5 g, 92.3 mmol), and stirred at -18°C for 1 h. The reaction mixture was diluted in AcOEt (500 mL) and washed with water {200 mL). The aqueous phase was separated and extracted with AcOEt (2 x 500 ml). The combined organic fractions were dried over Na.sum.SO/t, filtered and evaporated. The residue was purified by Combi-Flash Companion.(TM). (Isco Inc.) column chromatography (SiO2; gradient elution, [hexane / DCM 1 :1] / TBME 98:2 --> 6:4) to yield the title compound (13.0 g, 65.6 mmol, 78percent) as a pale yellow solid. MS: 199 [M+1]+ ; HPLC: \\et = 1.13; TLC: RF 0.39 (hexane / DCM / TBME 1 :1 :2).
60% With dihydrogen peroxide; 1-butylpyridinium bromide; toluene-4-sulfonic acid; In 1,2-dimethoxyethane; at 80℃; for 24h;Schlenk technique; Inert atmosphere; Green chemistry; General procedure: To a mixture of 2-aminopyridine (0.5 mmol, 1 equiv), p-TSA (0.4 mmol,0.8 equiv), 1-butylpyridinium bromide (1.5 mmol, 3 equiv) in a 50 mL Schlenk tube were added 1,2-dimethoxyethane (2 mL) under air. Then H2O2 (1.2 mmol, 2.4 equiv) was added. The mixture was stirred at 80°C for 24 h. And then the mixture was purified by silica gel column chromatography (petroleum ether/ethyl acetate) to give the products.
 

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