【结 构 式】 |
【分子编号】66825 【品名】ethyl 2-(8-carbamoyl-4-methyleneimidazo[5,1-d][1,2,3,5]tetrazin-3(4H)-yl)acetate 【CA登记号】 |
【 分 子 式 】C10H12N6O3 【 分 子 量 】264.244 【元素组成】C 45.45% H 4.58% N 31.80% O 18.16% |
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:(III)
【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