【结 构 式】 |
【分子编号】16856 【品名】3-iodo-4-isopropylbenzoic acid 【CA登记号】 |
【 分 子 式 】C10H11IO2 【 分 子 量 】290.10061 【元素组成】C 41.4% H 3.82% I 43.74% O 11.03% |
合成路线1
该中间体在本合成路线中的序号:(VIII)Cariporide has been obtained by two similar ways: 1) The oxidation of 4-isopropylbenzaldehyde (I) with sodium perborate in hot acetic acid gives 4-isopropylbenzoic acid (II), which is sulfonated with hot chlorosufonic acid yielding 3-(chlorosulfonyl)-4-isopropylbenzoic acid (III). The reduction of (III) with sodium sulfite in hot NaOH solution affords 4-isopropyl-3-sulfinobenzoic acid (IV), which is alkylated with methyl bromide and NaOH in DMF giving 4-isopropyl-3-(methylsulfonyl)benzoic acid (V). The reaction of (V) with SOCl2 in refluxing toluene yields 4-isopropyl-3-(methylsulfonyl)benzoyl chloride (VI), which is finally condensed with guanidine (VII) in DMF. 2) The iodination of 4-isopropylbenzoic acid (II) with iodine chloride or N-iodosuccinimide (NIS) gives 3-iodo-4-isopropylbenzoic acid (VIII), which is treated first with SOCl2 to afford the corresponding acyl chloride (IX), and then with methanol yielding 4-iodo-4-isopropylbenzoic methyl ester (X). The reaction of (X) with sodium methylsulfite (XI) gives 4-isopropyl-3-(methylsulfonyl)benzoic acid methyl ester (XII), which is finally treated with guanidine (VII) in refluxing THF.
【1】 Graul, A.; Prous, J.; Castañer, J.; Cariporide Mesylate. Drugs Fut 1997, 22, 11, 1197. |
【2】 Kleemann, H.-W.; Lang, H.-J.; Weichert, A.; Crause, P.; Scholz, W.; Albus, U.; Schwark, J.-R. (Aventis SA); Diacyl substd. guanidines, process for their preparation, their use as medicament or diagnostic reagent and medicament containing them. CA 2130703; DE 4328352; EP 0640587; JP 1995082234 . |
【3】 Lang, H.-J.; Weichert, A.; Kleemann, H.-W.; Englert, H.; Scholz, W.; Albus, U. (Aventis SA); Benzoylguanidines, process for their preparation and their use as antiarrhythmic agents. EP 0589336; JP 1994228082; US 5591754 . |
【4】 Kleemann, H.-W. (Aventis SA); Substd. benzoic acid esters, process for their preparation and their use for the synthesis of inhibitors of the cellular Na+/H+-exchange. DE 4428480 . |
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) | 23109 | 4-isopropylbenzaldehyde | 122-03-2 | C10H12O | 详情 | 详情 |
(II) | 11698 | 4-Isopropylbenzoic acid | 536-66-3 | C10H12O2 | 详情 | 详情 |
(III) | 16851 | 3-(chlorosulfonyl)-4-isopropylbenzoic acid | C10H11ClO4S | 详情 | 详情 | |
(IV) | 16852 | 3-(dioxo-lambda(6)-sulfanyl)-4-isopropylbenzoic acid | C10H12O4S | 详情 | 详情 | |
(V) | 16853 | 4-isopropyl-3-(methylsulfonyl)benzoic acid | C11H14O4S | 详情 | 详情 | |
(VI) | 16854 | 4-isopropyl-3-(methylsulfonyl)benzoyl chloride | C11H13ClO3S | 详情 | 详情 | |
(VII) | 14790 | Guanidine | 113-00-8 | CH5N3 | 详情 | 详情 |
(VIII) | 16856 | 3-iodo-4-isopropylbenzoic acid | C10H11IO2 | 详情 | 详情 | |
(IX) | 16857 | 3-iodo-4-isopropylbenzoyl chloride | C10H10ClIO | 详情 | 详情 | |
(X) | 16858 | methyl 3-iodo-4-isopropylbenzoate | C11H13IO2 | 详情 | 详情 | |
(XI) | 63963 | sodium methanesulfinate | CH3NaO2S | 详情 | 详情 | |
(XII) | 16859 | methyl 4-isopropyl-3-(methylsulfonyl)benzoate | C12H16O4S | 详情 | 详情 |