|
【结 构 式】 
|
【分子编号】22751 【品名】N-Methyldithiocarbamic acid sodium salt 【CA登记号】 |
【 分 子 式 】C2H4NNaS2 【 分 子 量 】129.182268 【元素组成】C 18.6% H 3.12% N 10.84% Na 17.8% S 49.64% |
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)The condensation of 7-aminocephalosporanic acid (I) with sodium 1,2,3-thiadiazole-5-thiolate (II) gives 7-amino-3-[1,2,3-thiadiazol-5-ylmethyl]-3-cephem-4-carboxylic acid (III). Following the first step, condensation of (III) with 2-(2-chloroacetamidothiazol-4-yl)-sulfanyl-(Z)-2-methoxyiminoacetyl chloride hydrochloride (IV) followed by deprotection with sodium N-methyldithiocarbamate (V) affords sodium 7-[(Z)-2-(2-aminothiazol-4yl)-2-(methoxyimino)acetamido)-3-(1,2,3-thiadiazol-5-ylsulfanylmethyl)-3-cephem-4-carboxylate.
| 【1】 Bietti, G.; Cereda, E.; Donetti, A.; Giachetti, A.; Pagani, F. (Angelini Inst SpA); Antiulcerogenic amidine derivatives of 2-substituted 4-phenylimidazole.. EP 0131973; GB 2149395; US 4649150 . |
| 【2】 Scarpignato, C.; Bisfentidine. Drugs Fut 1988, 13, 2, 110. |
| 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) | 22747 | (6R,7R)-3-[(acetoxy)methyl]-7-amino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid | C10H12N2O5S | 详情 | 详情 | |
| (II) | 22748 | 1,2,3-thiadiazol-5-thiol sodium salt | C2HN2NaS2 | 详情 | 详情 | |
| (III) | 22749 | (6R,7R)-7-amino-8-oxo-3-[(1,2,3-thiadiazol-5-ylsulfanyl)methyl]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid | C10H10N4O3S3 | 详情 | 详情 | |
| (IV) | 22750 | 2-[2-[(2-chloroacetyl)amino]-1,3-thiazol-5-yl]-2-(methoxyimino)acetyl chloride | C8H7Cl2N3O3S | 详情 | 详情 | |
| (V) | 22751 | N-Methyldithiocarbamic acid sodium salt | C2H4NNaS2 | 详情 | 详情 |
Extended Information