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HRID 2258388作成日:2026年10月25日
Diethylenetriamine → 3-[[[2-[(2-Aminoethyl)amino]ethyl]amino]acetylamino]-alpha-ethyl-2,4,6-triiodobenzenepropanoic acid
https://huagongshe.com/reaction/2258388
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Diethylenetriamine | HCID 8111 | — |
| 反応物 | 3-[(2-Chloroacetyl)amino]-alpha-ethyl-2,4,6-triiodobenzenepropanoic acid | HCID 22921389 | — |
| 生成物 | 3-[[[2-[(2-Aminoethyl)amino]ethyl]amino]acetylamino]-alpha-ethyl-2,4,6-triiodobenzenepropanoic acid | HCID 22921400 | 57% |
反応手順
To 217 g of diethylenetriamine (product commercially available) (2.1 mol), under stirring and under nitrogen atmosphere, 259 g of compound (A) 3-[(2-chloroacetyl) amino]-α-ethyl-2,4,6-triiodobenzenepropanoic acid (0.40 mol) are added. The mixture is kept at 50° C. for 3 h and, after cooling, is extracted with three 500-ml portions of CH2Cl2. After evaporation of the solvent, the residue is dissolved in 500 ml of H2O and acidified with 300 ml of 37% HCl. The resulting solution is counterflow extracted according to Craig with n-BuOH. A residue is obtained, which is purified as trihydrochloride by crystallisation in abs. EtOH after addition of 37% HCl. 187 g of 3-[[[2-[(2-aminoethyl)amino]ethyl]amino]acetylamino]-α-ethyl-2,4,6-triiodobenzenepropanoic acid (0.227 mol) are obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05660814 |
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| 出典データセット | uspto-grants-1997_08 |
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| ORD ID | ord-49f14293cea247b5a8680b1ddb1195bd |
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| 出典メモ | uspto-grants-1997_08 |
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