化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1590529作成日:2026年10月26日
Sodium Hydroxide → N,N'-Bis(1,3-dihydroxy-2-propyl)-5-[N-(2-hydroxy-3-methoxypropyl)acetamido]-2,4,6-triiodoisophthalamide
https://huagongshe.com/reaction/1590529
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 1-Chloro-3-methoxypropan-2-ol | HCID 97988 | — |
| 反応物 | Iopamidol ep impurity C | HCID 13140687 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Propylene Glycol | HCID 1030 | — |
| 生成物 | N,N'-Bis(1,3-dihydroxy-2-propyl)-5-[N-(2-hydroxy-3-methoxypropyl)acetamido]-2,4,6-triiodoisophthalamide | HCID 53648613 | — |
反応手順
5-Acetamido-N,N'-bis(1,3-dihydroxy-2-propyl)-2,4,6-triiodoisophthalamide (1036 g, 1.39 mol) was slurried in a mixture of propylene glycol (4170 ml) and methanol (4170 ml). After adding 18.25 M sodium hydroxide (114 ml, 2.08 mol), the mixture was heated at about 50°. When all or nearly all of the starting material was dissolved, the excess of methanol was evaporated in vacuo. Thereafter 2-hydroxy-3-methoxypropyl chloride (259 g, 2.08 mol) was added. The reaction mixture was heated at 50° for 44 hours and then stored at room temperature for 44 hours. Ater neutralization with concentrated hydrochloric acid, the reaction mixture was evaporated in vacuo. The residue was dissolved in methanol (3500 ml) and treated with a mixture of Dowex anion exchange resin 1×4 (2.87 kg) and Amberlite cation exchange resin (1.2 kg). The ion exchange resin was filtered off and washed with 80% aqueous methanol. The filtrate was evaporated in vacuo to dryness and the residue dissolved in isopropyl alcohol (5 1) at 80°. The product was precipitated by cooling to 13.5° and collected on a filter. Further purification was performed by recrystallization from isopropyl alcohol (4 1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05204086 |
|---|
| 出典データセット | uspto-grants-1993_04 |
|---|
| ORD ID | ord-f136ea4f0f6f43ea95ebb35458421e74 |
|---|
| 出典メモ | uspto-grants-1993_04 |
|---|