SU566842A1 - Method of preparing substituted imidazopyridines - Google Patents
Method of preparing substituted imidazopyridinesInfo
- 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
Links
Landscapes
- Nitrogen Condensed Heterocyclic Rings (AREA)
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.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU7602310356A SU566842A1 (en) | 1976-01-06 | 1976-01-06 | Method of preparing substituted imidazopyridines |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU7602310356A SU566842A1 (en) | 1976-01-06 | 1976-01-06 | Method of preparing substituted imidazopyridines |
Publications (1)
Publication Number | Publication Date |
---|---|
SU566842A1 true SU566842A1 (en) | 1977-07-30 |
Family
ID=20644302
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU7602310356A SU566842A1 (en) | 1976-01-06 | 1976-01-06 | Method of preparing substituted imidazopyridines |
Country Status (1)
Country | Link |
---|---|
SU (1) | SU566842A1 (en) |
Cited By (3)
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 |
-
1976
- 1976-01-06 SU SU7602310356A patent/SU566842A1/en active
Cited By (4)
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 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3781294A (en) | Certain dibenzo(b,f)thiepin(4,5-d) imidazoles | |
Wawzonek | Synthesis of pyrido [2, 3-d] pyrimidine-2, 4-diones | |
MXPA96005974A (en) | Improved process in the synthesis of n- [3- (3-cyanopyrazolo [1,5-a] pyrimidin-7-il) phenyl] -n-ethylacetam | |
McKay | The Preparation of N-Substituted-N1-nitroguanidines by the Reaction of Primary Amines with N-Alkyl-N-nitroso-N1-nitroguanidines | |
SU566842A1 (en) | Method of preparing substituted imidazopyridines | |
KR920000956B1 (en) | Process for the preparation of azulene derivarives | |
US3541101A (en) | Isoxazolo(5,4-b)pwridines,5,6 - polymethyleneisoxazolo(5,4 - b)pyridines and processes therefor | |
Bonacorso et al. | New efficient approach for the synthesis of 2‐alkyl (aryl) substituted 4H‐pyrido [1, 2‐a] pyrimidin‐4‐ones | |
SU521839A3 (en) | The method of obtaining benzophenone derivatives or their salts | |
SU654164A3 (en) | Method of obtaining aroylphenylindene or aroylphenylnaphthalene combinations derivatives or salts thereof | |
JPS60208963A (en) | Manufacture of diaminopyridine derivative | |
MAKI et al. | Photochemical Synthesis of Condensed Triazole N-Oxide | |
Noyce et al. | Studies of Configuration. V. The Preparation and Configuration of cis-3-Methoxycyclopentanecarboxylic Acid | |
SU623521A3 (en) | Method of obtaining triazolobenzothiazole | |
Yamazaki | Cyclization of isothiosemicarbazones. 5.[1, 2, 4] Triazolo [1, 5-c] pyrimidines | |
US3244725A (en) | 4, 5-diacyl-3-hydroxy-3-pyrrolin-2-ones | |
CA1089854A (en) | Pyrazolo[1,5-a]pyrido[4,3-d]pyrimidin-9(4h)- one and derivatives thereof | |
CA1051901A (en) | Derivatives of furo(2,3-d) pyrazolo(3,4-b) pyridines | |
US3278599A (en) | 2-(benzyloxyalkyl)-4-phenylimino-1, 3-cyclopentanedione derivatives | |
EP0279298B1 (en) | Tricyclic triazolopyrimidine derivatives | |
US2773872A (en) | Dihydroorotic acid | |
JPS5452047A (en) | Preparation of aromatic unsaturated ketones | |
SU486015A1 (en) | Method for preparing fused pyridinium compounds with a bridging nitrogen atom | |
Seidel | Preparation and reactions of some 2-oxo-2H-pyrido [1, 2-a] pyrimidines | |
SU514825A1 (en) | Method for preparing 1-phenyl-1-cyclohexyl-3- (1, -piperidino) -propanol-1 hydrochloride |