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【结 构 式】

【分子编号】62987

【品名】2-[(5-bromo-6-quinoxalinyl)imino]-4-imidazolidinone

【CA登记号】

【 分 子 式 】C11H8BrN5O

【 分 子 量 】306.12162

【元素组成】C 43.16% H 2.63% Br 26.1% N 22.88% O 5.23%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:AGN-192119

4) The reaction of amine (I) with phenyl cyanate (V) and KH in THF gives N-(5-bromoquinoxalin-6-yl)cyanamide (VI), which is cyclized with ethyl glycinate (VII) in refluxing ethanol to yield 2-(5-bromoquinoxalin-6-imino)imidazolidin-4-one (AGN-192119). 5) The reaction of cyanamide (VI) with 2-aminoacetaldehyde diethyl acetal (VIII) affords N1-(5-bromoquinoxalin-6-yl)-N3-(2,2-diethoxyethyl)guanidine (IX), which is cyclized by means of HCl to the hydroxyimidazoline (X). Finally, this compound is treated with NaOH to afford 5-bromo-6-(2-imidazolylamino)quinoxaline (AGN-192076).

1 Tang-Liu, D.; Burke, J.; Garst, M.; Harcourt, D.; Acheampong, A.; Breau, A.; Munk, S.A.; Wong, H.; Lai, R.; Wheeler, L.; Synthesis and characterization of degradation products and metabolites of brimonidine - A potent alpha2 adrenergic agonist. 211th ACS Natl Meet (March 24-28, New Orleans) 1996, Abst MEDI 021.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
AGN-192119 62987 2-[(5-bromo-6-quinoxalinyl)imino]-4-imidazolidinone C11H8BrN5O 详情 详情
AGN-192076 62988 5-bromo-N-(1H-imidazol-2-yl)-6-quinoxalinamine; N-(5-bromo-6-quinoxalinyl)-N-(1H-imidazol-2-yl)amine C11H8BrN5 详情 详情
(I) 10328 5-Bromo-6-quinoxalinamine; 5-Bromo-6-quinoxalinylamine C8H6BrN3 详情 详情
(V) 62986 phenyl cyanate C7H5NO 详情 详情
(VI) 10330 N-(5-Bromo-6-quinoxalinyl)cyanamide C9H5BrN4 详情 详情
(VII) 10309 ethyl 2-aminoacetate; Glycine ethyl ester 459-73-4 C4H9NO2 详情 详情
(VIII) 10331 2,2-Diethoxy-1-ethanamine; 2,2-Diethoxyethylamine; Aminoacetaldehyde diethyl acetal 645-36-3 C6H15NO2 详情 详情
(IX) 10332 N-(5-Bromo-6-quinoxalinyl)-N'-(2,2-diethoxyethyl)guanidine C15H20BrN5O2 详情 详情
(X) 10333 2-[(5-Bromo-6-quinoxalinyl)amino]-4,5-dihydro-1H-imidazol-5-ol C11H10BrN5O 详情 详情
Extended Information