RU2012155395A - METHOD FOR PRODUCING 3-ARYL-1,5,3-DITIAZOCANES - Google Patents

METHOD FOR PRODUCING 3-ARYL-1,5,3-DITIAZOCANES Download PDF

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RU2012155395A
RU2012155395A RU2012155395/04A RU2012155395A RU2012155395A RU 2012155395 A RU2012155395 A RU 2012155395A RU 2012155395/04 A RU2012155395/04 A RU 2012155395/04A RU 2012155395 A RU2012155395 A RU 2012155395A RU 2012155395 A RU2012155395 A RU 2012155395A
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aryl
arylamine
tetramethyl
diamine
cucl
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RU2012155395/04A
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RU2538600C2 (en
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Усеин Меметович Джемилев
Асхат Габдрахманович Ибрагимов
Леонард Мухибович Халилов
Наталия Наильевна Махмудиярова
Кирилл Игоревич Прокофьев
Лилия Вазилевна Мударисова
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Федеральное государственное бюджетное учреждение науки Институт нефтехимии и катализа Российской академии наук
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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Thiazole And Isothizaole Compounds (AREA)

Abstract

Способ получения 3-арил-1,5,3-дитиазоканов общей формулы (1a-i)отличающийся тем, что N,N,N,N-тетраметил-2,6-дитиагептан-1,7-диамин подвергают взаимодействию с ариламином (арил - фенил, m- и p-метилфенил, o-, m- и p-метоксифенил, o-, m- и p-нитрофенил) в присутствии катализатора CuClв мольном соотношении N,N,N,N-тетраметил-2,6-дитиагептан-1,7-диамин:ариламин:CuCl=10:10:(0.3-0.7) при температуре ~60°С и атмосферном давлении в хлороформе в качестве растворителя в течение 60-90 мин.A method of obtaining 3-aryl-1,5,3-dithiazocanes of the general formula (1a-i) characterized in that N, N, N, N-tetramethyl-2,6-dithiaheptan-1,7-diamine is reacted with an arylamine ( aryl - phenyl, m- and p-methylphenyl, o-, m- and p-methoxyphenyl, o-, m- and p-nitrophenyl) in the presence of a CuCl catalyst in a molar ratio of N, N, N, N-tetramethyl-2.6 -dithiaheptane-1,7-diamine: arylamine: CuCl = 10: 10: (0.3-0.7) at a temperature of ~ 60 ° C and atmospheric pressure in chloroform as a solvent for 60-90 min.

Claims (1)

Способ получения 3-арил-1,5,3-дитиазоканов общей формулы (1a-i)The method of obtaining 3-aryl-1,5,3-dithiazocanes of the general formula (1a-i)
Figure 00000001
Figure 00000001
отличающийся тем, что N1,N1,N7,N7-тетраметил-2,6-дитиагептан-1,7-диамин подвергают взаимодействию с ариламином (арил - фенил, m- и p-метилфенил, o-, m- и p-метоксифенил, o-, m- и p-нитрофенил) в присутствии катализатора CuCl2 в мольном соотношении N1,N1,N7,N7-тетраметил-2,6-дитиагептан-1,7-диамин:ариламин:CuCl2=10:10:(0.3-0.7) при температуре ~60°С и атмосферном давлении в хлороформе в качестве растворителя в течение 60-90 мин. characterized in that N 1 , N 1 , N 7 , N 7- tetramethyl-2,6-dithiaheptan-1,7-diamine are reacted with arylamine (aryl-phenyl, m- and p-methylphenyl, o-, m- and p-methoxyphenyl, o-, m- and p-nitrophenyl) in the presence of a CuCl 2 catalyst in a molar ratio of N 1 , N 1 , N 7 , N 7- tetramethyl-2,6-dithiaheptan-1,7-diamine: arylamine : CuCl 2 = 10: 10: (0.3-0.7) at a temperature of ~ 60 ° C and atmospheric pressure in chloroform as a solvent for 60-90 minutes.
RU2012155395/04A 2012-12-19 2012-12-19 Method of obtaining 3-aryl-1,5,3-dithiazocanes RU2538600C2 (en)

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RU2626006C1 (en) * 2016-02-02 2017-07-21 Федеральное государственное бюджетное учреждение науки Институт нефтехимии и катализа Российской академии наук Method of producing 4-(o,m,p-halogenphenyl)-2,6-dithia-4-azabicyclo [5,3,1]undeca-1(11),7,9-trienes

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RU2467002C1 (en) * 2011-05-30 2012-11-20 Учреждение Российской Академии Наук Институт Нефтехимии И Катализа Ран METHOD OF OBTAINING 3-(o-,m-,p-NITROPHENYL)-TETRAHYDRO-2H,6H-1,5,3-DITHIAZOCENES
RU2467001C1 (en) * 2011-05-30 2012-11-20 Учреждение Российской Академии Наук Институт Нефтехимии И Катализа Ран METHOD OF OBTAINING 3-(o-,m-,p-METHOXYPHENYL)-TETRAHYDRO-2H, 6H-1, 5, 3-DITHIAZOCENES
RU2467000C1 (en) * 2011-05-30 2012-11-20 Учреждение Российской Академии Наук Институт Нефтехимии И Катализа Ран Method of obtaining 3-aryl-tetrahydro-2h,6h-1,5,3-dithiazocines

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