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【结 构 式】

【分子编号】66820

【品名】5-amino-1H-imidazole-4-carboxamide hydrochloride

【CA登记号】21299-72-9

【 分 子 式 】C4H6N4O.HCl

【 分 子 量 】162.579

【元素组成】C 29.55% H 4.34% Cl 21.81% N 34.46% O 9.84%

与该中间体有关的原料药合成路线共 4 条

合成路线1

该中间体在本合成路线中的序号:(IV)

 

1 Ku SC. 2002. A process tor the prepn. of temoiolomide and its analogs via the oxiadative cyclization of 5-amino-4-aminocarbonylirmdazolylbyrkuides. W0 2002057268
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 66818 2-amino-2-cyanoacetamide;Aminocyanacetamide 6719-21-7 C3H5N3O 详情 详情
(II) 66815 (E)-N,N'-bis(methylcarbamoyl)formimidamide   C5H10N4O2 详情 详情
(III) 66819 5-amino-N1-methyl-1H-imidazole-1,4-dicarboxamide   C6H9N5O2 详情 详情
(IV) 66820 5-amino-1H-imidazole-4-carboxamide hydrochloride 21299-72-9 C4H6N4O.HCl 详情 详情
(V) 66811 2-amino-N-(tert-butyl)-2-cyanoacetamide   C7H13N3O 详情 详情
(VI) 66816 5-amino-N4-(tert-butyl)-N1-methyl-1H-imidazole-1,4-dicarboxamide   C10H17N5O2 详情 详情
(VII) 66821 4-nitrophenyl 5-amino-4-carbamoyl-1H-imidazole-1-carboxylate   C11H9N5O5 详情 详情
(VIII) 66822 5-amino-1-(1-methylhydrazinecarbonyl)-1H-imidazole-4-carboxamide   C6H10N6O2 详情 详情

合成路线2

该中间体在本合成路线中的序号:(I)

 

1 Stevens MF, Hickman JA, StoneR,et al.1984. Antitumour imidazotetnzines. 1. Synthesis an chemistry of 8-carbamoyl-3-(2-chloroethyl) imidazo[5,1-d] -1,2,3,5-tetrazirr4(3H) -one.a novel broad-spectrum antitumor agent. J Med Chem, 27(2):196~201
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 66820 5-amino-1H-imidazole-4-carboxamide hydrochloride 21299-72-9 C4H6N4O.HCl 详情 详情
(II) 56930 4-diazo-4H-imidazole-5-carboxamide C4H3N5O 详情 详情

合成路线3

该中间体在本合成路线中的序号:(I)

 

1 Wang YF, Stevens MF. 1996. Synthetic studies of 8-arbamoylimidazo-[5,l-D] -1,2,3,5-tetnzin-4(3H)-one: a key derivative of antitumor drug ternozolomide. Bioorg Med Chem lett, 6(2):185~188
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 66820 5-amino-1H-imidazole-4-carboxamide hydrochloride 21299-72-9 C4H6N4O.HCl 详情 详情
(II) 56930 4-diazo-4H-imidazole-5-carboxamide C4H3N5O 详情 详情
(III) 66823 4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxamide   C5H4N6O2 详情 详情

合成路线4

该中间体在本合成路线中的序号:(I)

 

1 Wang YF, Stevens MF, Thomson W. 1994. Altemative syntheses of the antitumor drug temozolomide avoiding the use of methyl isocyanate. Journal of the Chemical Society, Chenucal Communications, (14): 1687~1688.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 66820 5-amino-1H-imidazole-4-carboxamide hydrochloride 21299-72-9 C4H6N4O.HCl 详情 详情
(II) 66824 ethyl 2-(5-amino-4-carbamoyl-1H-imidazole-1-carboxamido)acetate hydrochloride   C9H13N5O4.HCl 详情 详情
(III) 66825 ethyl 2-(8-carbamoyl-4-methyleneimidazo[5,1-d][1,2,3,5]tetrazin-3(4H)-yl)acetate   C10H12N6O3 详情 详情
(IV) 66826 2-(8-carbamoyl-4-methyleneimidazo[5,1-d][1,2,3,5]tetrazin-3(4H)-yl)acetic acid   C8H8N6O3 详情 详情
(V) 66827 2-thioxopyridin-1(2H)-yl 2-(8-carbamoyl-4-methyleneimidazo[5,1-d][1,2,3,5]tetrazin-3(4H)-yl)acetate   C13H11N7O3S 详情 详情
Extended Information