Reaction of 5-nitrospiro[benzimidazole-2,1′-cyclohexane] 1,3-dioxide with electrophilic reagents: Bromine and nitric acid

Reactions of 5-nitrospiro[benzimidazole-2,1′-cyclohexane] 1,3-dioxide with bromine and nitric acid lead to the electrophilic substitution of the hydrogen atom in the meta -position with respect to the nitro group. At thebromination the primarily formed 4-bromo-6-nitrospiro[benzimidazole-2,1′-cyclohe...

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Vydáno v:Russian journal of organic chemistry Ročník 49; číslo 8; s. 1208 - 1214
Hlavní autoři: Samsonov, V. A., Gatilov, Yu. V., Savel’ev, V. A.
Médium: Journal Article
Jazyk:angličtina
Vydáno: Boston Springer US 01.08.2013
Springer Nature
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ISSN:1070-4280, 1608-3393
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Abstract Reactions of 5-nitrospiro[benzimidazole-2,1′-cyclohexane] 1,3-dioxide with bromine and nitric acid lead to the electrophilic substitution of the hydrogen atom in the meta -position with respect to the nitro group. At thebromination the primarily formed 4-bromo-6-nitrospiro[benzimidazole-2,1′-cyclohexane] 1,3-dioxide when kept in the solution loses an oxygen atom forming 4-bromo-6-nitrospiro[benzimidazole-2,1′-cyclohexane] 1-oxide and an isomerization product, 8-bromo-6-nitrospiro[3 H -[2,1,4]benzoxadiazine-3,1′-cyclohexane] 4-oxide. The latter exposed to light turns into 4-bromo-6-nitrospiro[benzimidazole-2,1′-cyclohexane] 1,3-dioxide. The reaction of the initial 1,3-dioxide with nitric acid afforded 4,6-dinitrospiro[benzimidazole-2,1′-cyclohexan]-7-ol 1-oxide whose heating in o -dichlorobenzene resulted in 3,5-dinitro-1,8-diazatricyclo[7.5.0.0 2,7 ] tetradeca-2(7),3,5,8-tetraen-6-ol.
AbstractList Reactions of 5-nitrospiro[benzimidazole-2,1'-cyclohexane] 1,3-dioxide with bromine and nitric acid lead to the electrophilic substitution of the hydrogen atom in the meta-position with respect to the nitro group. At thebromination the primarily formed 4-bromo-6-nitrospiro[benzimidazole-2,1'-cyclohexane] 1,3-dioxide when kept in the solution loses an oxygen atom forming 4-bromo-6-nitrospiro[benzimidazole-2,1'-cyclohexane] 1-oxide and an isomerization product, 8-bromo-6-nitrospiro[3H-[2,1,4]benzoxadiazine-3,1'-cyclohexane] 4-oxide. The latter exposed to light turns into 4-bromo-6-nitrospiro[benzimidazole-2,1'-cyclohexane] 1,3-dioxide. The reaction of the initial 1,3-dioxide with nitric acid afforded 4,6-dinitrospiro[benzimidazole-2,1'-cyclohexan]-7-ol 1-oxide whose heating in o-dichlorobenzene resulted in 3,5-dinitro-1,8-diazatricyclo[7.5.0.0(2,7)] tetradeca-2(7),3,5,8-tetraen-6-ol.
Reactions of 5-nitrospiro[benzimidazole-2,1′-cyclohexane] 1,3-dioxide with bromine and nitric acid lead to the electrophilic substitution of the hydrogen atom in the meta -position with respect to the nitro group. At thebromination the primarily formed 4-bromo-6-nitrospiro[benzimidazole-2,1′-cyclohexane] 1,3-dioxide when kept in the solution loses an oxygen atom forming 4-bromo-6-nitrospiro[benzimidazole-2,1′-cyclohexane] 1-oxide and an isomerization product, 8-bromo-6-nitrospiro[3 H -[2,1,4]benzoxadiazine-3,1′-cyclohexane] 4-oxide. The latter exposed to light turns into 4-bromo-6-nitrospiro[benzimidazole-2,1′-cyclohexane] 1,3-dioxide. The reaction of the initial 1,3-dioxide with nitric acid afforded 4,6-dinitrospiro[benzimidazole-2,1′-cyclohexan]-7-ol 1-oxide whose heating in o -dichlorobenzene resulted in 3,5-dinitro-1,8-diazatricyclo[7.5.0.0 2,7 ] tetradeca-2(7),3,5,8-tetraen-6-ol.
Author Gatilov, Yu. V.
Samsonov, V. A.
Savel’ev, V. A.
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Cites_doi 10.1021/jp953141+
10.1107/S0108767307043930
10.1016/j.ejmech.2009.06.014
10.1134/S1070428012030116
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Keywords Bromine
Furoxane
Benzimidazole
Cyclohexane
Electrophilic Substitution
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References Khmel’nitskiiLINovikovSSGodovikovaTIKhimiya furoksanov. Reaktsii i primenenie1996MoscowNauka(Furoxane Chemistry)
SamsonovVABagryanskayaIYuGatilovYuSavel’evVAIzv. Akad. Nauk,^Ser. Khim.20111697
SuschitzkyHCroat. Chem. Acta19865957
SheldrickGMActa, Cryst. A20086411210.1107/S01087673070439301:CAS:528:DC%2BD2sXhsVGhurzO
SamsonovVAVolodarskiiLBShamirzaevaOVKhim Geterotsikl. Soedin.1994524
SamsonovVAGatilovYuASavel’evVABaranovaSSZh. Org. Khim.201248403
RowlandRSTaylorRJ. Phys. Chem.1996100738410.1021/jp953141+1:CAS:528:DyaK28Xit1ykt7k%3D
BoianiMBoianiLMerlinoAHernandezPChidichimoACazzuloJJCerecettoHGonzalezMEur. J. Med. Chem.200944442610.1016/j.ejmech.2009.06.0141:CAS:528:DC%2BD1MXht1Ggtb3O
M Boiani (418_CR2) 2009; 44
RS Rowland (418_CR5) 1996; 100
VA Samsonov (418_CR4) 2011
LI Khmel’nitskii (418_CR6) 1996
H Suschitzky (418_CR1) 1986; 59
VA Samsonov (418_CR7) 1994
VA Samsonov (418_CR3) 2012; 48
GM Sheldrick (418_CR8) 2008; 64
SAMSONOV, VA (WOS:A1994NZ62500015) 1994
SAMSONOV VA 2011
Sheldrick, GM (WOS:000251924000011) 2008; 64
SUSCHITSKY, H (WOS:A1986C881600007) 1986; 59
Rowland, RS (WOS:A1996UJ11700012) 1996; 100
SAMSONOV VA 2012; 0048
Boiani, M (WOS:000271225800018) 2009; 44
Khmel'nitskii, L.I. (000324112500019.2) 1996
References_xml – reference: SheldrickGMActa, Cryst. A20086411210.1107/S01087673070439301:CAS:528:DC%2BD2sXhsVGhurzO
– reference: SamsonovVAGatilovYuASavel’evVABaranovaSSZh. Org. Khim.201248403
– reference: SamsonovVABagryanskayaIYuGatilovYuSavel’evVAIzv. Akad. Nauk,^Ser. Khim.20111697
– reference: SuschitzkyHCroat. Chem. Acta19865957
– reference: SamsonovVAVolodarskiiLBShamirzaevaOVKhim Geterotsikl. Soedin.1994524
– reference: BoianiMBoianiLMerlinoAHernandezPChidichimoACazzuloJJCerecettoHGonzalezMEur. J. Med. Chem.200944442610.1016/j.ejmech.2009.06.0141:CAS:528:DC%2BD1MXht1Ggtb3O
– reference: Khmel’nitskiiLINovikovSSGodovikovaTIKhimiya furoksanov. Reaktsii i primenenie1996MoscowNauka(Furoxane Chemistry)
– reference: RowlandRSTaylorRJ. Phys. Chem.1996100738410.1021/jp953141+1:CAS:528:DyaK28Xit1ykt7k%3D
– volume: 100
  start-page: 7384
  year: 1996
  ident: 418_CR5
  publication-title: J. Phys. Chem.
  doi: 10.1021/jp953141+
– start-page: 524
  volume-title: Khim Geterotsikl. Soedin.
  year: 1994
  ident: 418_CR7
– volume: 48
  start-page: 403
  year: 2012
  ident: 418_CR3
  publication-title: Zh. Org. Khim.
– volume: 64
  start-page: 112
  year: 2008
  ident: 418_CR8
  publication-title: Acta, Cryst. A
  doi: 10.1107/S0108767307043930
– volume-title: Khimiya furoksanov. Reaktsii i primenenie
  year: 1996
  ident: 418_CR6
– volume: 44
  start-page: 4426
  year: 2009
  ident: 418_CR2
  publication-title: Eur. J. Med. Chem.
  doi: 10.1016/j.ejmech.2009.06.014
– start-page: 1697
  volume-title: Izv. Akad. Nauk,^Ser. Khim.
  year: 2011
  ident: 418_CR4
– volume: 59
  start-page: 57
  year: 1986
  ident: 418_CR1
  publication-title: Croat. Chem. Acta
– volume: 0048
  start-page: 00403
  year: 2012
  publication-title: ZH ORG KHIM
  doi: 10.1134/S1070428012030116
– volume: 64
  start-page: 112
  year: 2008
  ident: WOS:000251924000011
  article-title: A short history of SHELX
  publication-title: ACTA CRYSTALLOGRAPHICA A-FOUNDATION AND ADVANCES
  doi: 10.1107/S0108767307043930
– volume: 59
  start-page: 57
  year: 1986
  ident: WOS:A1986C881600007
  article-title: THE 2H-BENZIMIDAZOLES (ISOBENZIMIDAZOLES) AS SYNTHONS IN HETEROCYCLIC CHEMISTRY
  publication-title: CROATICA CHEMICA ACTA
– start-page: 524
  year: 1994
  ident: WOS:A1994NZ62500015
  article-title: FORMATION OF 2H-BENZIMIDAZOLE-1,3-DIOXIDES AT INTERACTION OF BENZOFUROXANS WITH ALCOHOLS AND ALKYL-HALIDES IN THE PRESENCE OF ACIDS
  publication-title: KHIMIYA GETEROTSIKLICHESKIKH SOEDINENII
– volume: 44
  start-page: 4426
  year: 2009
  ident: WOS:000271225800018
  article-title: Second generation of 2H-benzimidazole 1,3-dioxide derivatives as anti-trypanosomatid agents: Synthesis, biological evaluation, and mode of action studies
  publication-title: EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
  doi: 10.1016/j.ejmech.2009.06.014
– year: 1996
  ident: 000324112500019.2
  article-title: Khimiya furoksanov. Reaktsii i primenenie
  publication-title: Furoxane Chemistry
– volume: 100
  start-page: 7384
  year: 1996
  ident: WOS:A1996UJ11700012
  article-title: Intermolecular nonbonded contact distances in organic crystal structures: Comparison with distances expected from van der Waals radii
  publication-title: JOURNAL OF PHYSICAL CHEMISTRY
– start-page: 01697
  year: 2011
  publication-title: IZV AKAD NAUK SSSR K
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Reactions of 5-nitrospiro[benzimidazole-2,1'-cyclohexane] 1,3-dioxide with bromine and nitric acid lead to the electrophilic substitution of the hydrogen atom...
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Title Reaction of 5-nitrospiro[benzimidazole-2,1′-cyclohexane] 1,3-dioxide with electrophilic reagents: Bromine and nitric acid
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