【结 构 式】 |
【分子编号】21932 【品名】methyl 5-[(2-imino-4-oxo-1,3-thiazolidin-5-yl)methyl]-2-methoxybenzoate 【CA登记号】 |
【 分 子 式 】C13H14N2O4S 【 分 子 量 】294.33124 【元素组成】C 53.05% H 4.79% N 9.52% O 21.74% S 10.89% |
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:(XII)2) An alternative method starting from aniline (VII) employed the Meerwein arylation of methyl acrylate (IX) with the intermediate diazonium salt (VIII) in the presence of cuprous oxide. The resulting bromoester (X) was cyclized with thiourea (XI) in Et2O, followed by hydrolysis with HCl in sulfolane to afford (XIII). Finally, acid (XIII) was coupled to benzylamine (V) in the presence of (EtO)2POCN and Et3N.
【1】 Nomura, M.; et al.; (3-Substituted benzyl)thiazolidine-2,4-diones as structurally new antihyperglycemic agents. Bioorg Med Chem Lett 1999, 9, 4, 533. |
中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
---|---|---|---|---|---|---|
42235 | Diethyl phosphorocyanidate; Diethyl cyanophosphonate; Cyanophosphonic acid diethyl ester; Diethyl phosphoryl cyanide; DEPC | 2942-58-7 | C5H10NO3P | 详情 | 详情 | |
(V) | 21925 | [4-(trifluoromethyl)phenyl]methanamine; 4-(trifluoromethyl)benzylamine | 3300-51-4 | C8H8F3N | 详情 | 详情 |
(VII) | 21927 | methyl 5-amino-2-methoxybenzoate | C9H11NO3 | 详情 | 详情 | |
(VIII) | 21928 | methyl 5-(1lambda(5)-diazynyl)-2-methoxybenzoate | C9H10N2O3 | 详情 | 详情 | |
(IX) | 14156 | methyl acrylate | 96-33-3 | C4H6O2 | 详情 | 详情 |
(X) | 21930 | methyl 5-(2-bromo-3-methoxy-3-oxopropyl)-2-methoxybenzoate | C13H15BrO5 | 详情 | 详情 | |
(XI) | 10180 | Thiourea | 62-56-6 | CH4N2S | 详情 | 详情 |
(XII) | 21932 | methyl 5-[(2-imino-4-oxo-1,3-thiazolidin-5-yl)methyl]-2-methoxybenzoate | C13H14N2O4S | 详情 | 详情 | |
(XIII) | 21933 | 5-[(2,4-dioxo-1,3-thiazolidin-5-yl)methyl]-2-methoxybenzoic acid | C12H11NO5S | 详情 | 详情 |
Extended Information