SU566842A1 - Method of preparing substituted imidazopyridines - Google Patents

Method of preparing substituted imidazopyridines

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Publication number
SU566842A1
SU566842A1 SU7602310356A SU2310356A SU566842A1 SU 566842 A1 SU566842 A1 SU 566842A1 SU 7602310356 A SU7602310356 A SU 7602310356A SU 2310356 A SU2310356 A SU 2310356A SU 566842 A1 SU566842 A1 SU 566842A1
Authority
SU
USSR - Soviet Union
Prior art keywords
preparing substituted
substituted imidazopyridines
imidazopyridines
pyridip
imidazo
Prior art date
Application number
SU7602310356A
Other languages
Russian (ru)
Inventor
Юрий Михайлович Ютилов
Любовь Ивановна Ковалева
Original Assignee
Донецкое Отделение Физико-Органической Химии Института Физической Химии Им.Л.В.Писаржевского Ан Украинской Сср
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Application filed by Донецкое Отделение Физико-Органической Химии Института Физической Химии Им.Л.В.Писаржевского Ан Украинской Сср filed Critical Донецкое Отделение Физико-Органической Химии Института Физической Химии Им.Л.В.Писаржевского Ан Украинской Сср
Priority to SU7602310356A priority Critical patent/SU566842A1/en
Application granted granted Critical
Publication of SU566842A1 publication Critical patent/SU566842A1/en

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Description

Пример 1. Получение 2-фенилимидазо 4,5-с пиридина (соединение № 1).Example 1. The preparation of 2-phenylimidazo 4,5-c pyridine (compound No. 1).

Смесь, состо вшую из эквимолекул рных количеств 3,4-диаминопиридина, бензальдегида и серы, нагревают 4 ч ири 170-175°С, охлаждают до комнатной темиературы и продукт реакции кристаллизуют из водного спирта. Т. пл. 227°С. Выход 91%.A mixture consisting of equimolecular amounts of 3,4-diaminopyridine, benzaldehyde and sulfur is heated for 4 hours with 170-175 ° C, cooled to room temperature and the reaction product is crystallized from aqueous alcohol. T. pl. 227 ° C. Yield 91%.

В случае проведени  реакции в растворителе (мезитилен) на 1 вес. ч. серы берут 25 вес. ч. мезитилена. Реакцию провод т при температуре кипепи  реакционной массы 2-4 ч. Осадок после охлаждени  отфильтровывают и очищают кристаллизацией.If the reaction is carried out in a solvent (mesitylene) by 1 weight. h. sulfur take 25 weight. h. mesitylene. The reaction is carried out at the boiling point of the reaction mass for 2-4 hours. After cooling, the precipitate is filtered off and purified by crystallization.

Аналогично примеру 1 с использованием соответствующих исходных продуктов при нагревании в течение 1-6 ч при 150-175°С получены следующие целевые соединени :Analogously to Example 1, using the corresponding starting materials, the following target compounds were obtained by heating for 1-6 hours at 150-175 ° C:

№22- (4 - диметиламинофенил) -имидазо 4,5-с пиридип;No. 22- (4 - dimethylaminophenyl) -imidazo 4,5-c pyridip;

№ 3 2 - (4-метоксифенил)-имидазо 4,5-с пиридин;No. 3 2- (4-methoxyphenyl) -imidazo 4,5-c pyridine;

№ 4 1 - метил-2-(1-метилиндолил-2)-имидазо 4 ,5-Ь пиридип;No. 4 1 - methyl-2- (1-methylindolyl-2) -imidazo 4, 5-b pyridip;

№ 5 2 - фенилимидазо 4,5-Ь пиридип;No. 5 2 - phenylimidazo 4,5-b pyridip;

№ 6 2 - 4-(диметиламино)-фенил -5-хлоримидазо 4,5-& пиридин.No. 6 2 - 4- (dimethylamino) -phenyl-5-chlorimidazo 4,5- & pyridine.

Свойства полученных соединений приведены в таблице.Properties of the compounds obtained are shown in the table.

SU7602310356A 1976-01-06 1976-01-06 Method of preparing substituted imidazopyridines SU566842A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU7602310356A SU566842A1 (en) 1976-01-06 1976-01-06 Method of preparing substituted imidazopyridines

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Application Number Priority Date Filing Date Title
SU7602310356A SU566842A1 (en) 1976-01-06 1976-01-06 Method of preparing substituted imidazopyridines

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4603139A (en) * 1981-11-10 1986-07-29 Burroughs Wellcome Co. Bicycle compounds, processes for their preparation and pharmaceutical formulations containing compounds
US4616090A (en) * 1981-08-19 1986-10-07 Merck Patent Gesellschaft Mit Beschrankter Haftung 2-arylimidazopyridines intermediates
RU2498984C2 (en) * 2007-09-12 2013-11-20 Сентр Насьональ Де Ла Решерш Сьентифик Perharidines as cdk inihibitors

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4616090A (en) * 1981-08-19 1986-10-07 Merck Patent Gesellschaft Mit Beschrankter Haftung 2-arylimidazopyridines intermediates
US5104881A (en) * 1981-08-19 1992-04-14 Merck Patent Gesellschaft Mit Beschrankter Haftung 2-arylimidazopyridines
US4603139A (en) * 1981-11-10 1986-07-29 Burroughs Wellcome Co. Bicycle compounds, processes for their preparation and pharmaceutical formulations containing compounds
RU2498984C2 (en) * 2007-09-12 2013-11-20 Сентр Насьональ Де Ла Решерш Сьентифик Perharidines as cdk inihibitors

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