【结 构 式】 |
【分子编号】56515 【品名】2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetyl 4-methylbenzenesulfonate 【CA登记号】 |
【 分 子 式 】C13H13N3O5S2 【 分 子 量 】355.39544 【元素组成】C 43.94% H 3.69% N 11.82% O 22.51% S 18.05% |
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:(V)In a further procedure, 2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetic acid (IV) was activated as the mixed anhydride (V) by treatment with tosyl chloride and triethylamine. After protection of the cephem thioether (III) by silylation with either chlorotrimethylsilane or with bis(trimethylsilyl)acetamide, coupling with the mixed anhydride (V) gave rise to the title compound.
【1】 Wagner, H.; Jaenicke, O.; Worm, M. (Aventis Pharma AG); Process for the preparation of cefodizime. EP 0226093 . |
中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
---|---|---|---|---|---|---|
(III) | 56514 | 7-amino-3-({[5-(carboxymethyl)-4-methyl-1,3-thiazol-2-yl]sulfanyl}methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid | C14H15N3O5S3 | 详情 | 详情 | |
(IV) | 24737 | 2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetic acid | 65872-41-5 | C6H7N3O3S | 详情 | 详情 |
(V) | 56515 | 2-(2-amino-1,3-thiazol-4-yl)-2-(methoxyimino)acetyl 4-methylbenzenesulfonate | C13H13N3O5S2 | 详情 | 详情 |
Extended Information