【结 构 式】 |
【分子编号】60035 【品名】1,4,7,10-tetraazabicyclo[8.2.2]tetradecan-11-one 【CA登记号】 |
【 分 子 式 】C10H20N4O 【 分 子 量 】212.29516 【元素组成】C 56.58% H 9.5% N 26.39% O 7.54% |
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:(XVI)A different synthesis started from the previously reported tetraaza cyclopentaacenaphthylene (XV). Treatment of (XV) with a solution of piperazine at pH 6 gave rise to the bicyclic lactam (XVI). Alkylation of (XVI) with bromoacetic acid, followed by basic lactam hydrolysis furnished the tris(carboxymethyl) derivative (X), which was processed as in Scheme 3.
【1】 Argese, M.; Ripa, G. (Bracco SpA; Dibra SpA); 1,4,7,10-Tetraazabicyclo[8.2.2]tetradecan-2-one, a process for the preparation thereof and the use thereof for the preparation of tetraazamacrocycles. EP 0998476; JP 2002511884; WO 9905145 . |
中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
---|---|---|---|---|---|---|
(A) | 23660 | 2-Bromoacetic acid | 79-08-3 | C2H3BrO2 | 详情 | 详情 |
(X) | 60030 | trisodium 2-[4,10-bis(2-oxido-2-oxoethyl)-1,4,7,10-tetraazacyclododecan-1-yl]acetate | C14H23N4Na3O6 | 详情 | 详情 | |
(XV) | 60034 | 1,4,7,10-tetraazatricyclo[8.2.2.2~4,7~]hexadecane | C12H24N4 | 详情 | 详情 | |
(XVI) | 60035 | 1,4,7,10-tetraazabicyclo[8.2.2]tetradecan-11-one | C10H20N4O | 详情 | 详情 | |
(XVII) | 60036 | 2-[7-(2-hydroxy-2-oxoethyl)-11-oxo-1,4,7,10-tetraazabicyclo[8.2.2]tetradec-4-yl]acetic acid | C14H24N4O5 | 详情 | 详情 |
Extended Information