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【结 构 式】
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【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