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N-Cyclohexyl-1,3-propanediamine → N-(3'-Cyclohexylaminopropyl)-aspartic acid-4-isopropyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | N-Cyclohexyl-1,3-propanediamine | HCID 18718 | — |
| 反応物 | Monoisopropyl maleate | HCID 6436106 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | N-(3'-Cyclohexylaminopropyl)-aspartic acid-4-isopropyl ester | HCID 22817117 | 82.2% |
反応手順
In a manner analogous to that of Example 1, 400 ml of triethylamine are added to 350.2 g (2.0 mols+10% excess) of maleic acid-monoisopropyl ester, and the mixture is subsequently reacted with 311.3 g (2.0 mols) of 3-cyclohexylamino-1-propylamine at 59°-85° C. for 35 minutes. The reaction mixture is further processed in the manner described in Example 1 to yield 515 g (82.2% of theory) of the desired aspartic acid derivative, which decomposes at 151°-152° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04284755 |
| 出典データセット | uspto-grants-1981_08 |
| ORD ID | ord-cd2d0730f3d64e0d8062d58cab844f18 |
| 出典メモ | uspto-grants-1981_08 |