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N,N-Dimethyl-1,3-propanediamine → N-(3'-Dimethylaminopropyl)-aspartic acid-4-cyclohexyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | N,N-Dimethyl-1,3-propanediamine | HCID 7993 | — |
| 反応物 | 1-Cyclohexyl (2Z)-2-butenedioate | HCID 6913007 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | N-(3'-Dimethylaminopropyl)-aspartic acid-4-cyclohexyl ester | HCID 86738345 | 73.2% |
反応手順
In a manner analogous to that described in Example 1, 100 ml of triethylamine are added dropwise, with cooling, to 99.1 g (0.5 mol) of maleic acid-monocyclohexyl ester, and the mixture is reacted with 61.3 g (0.5 mol+20% excess) of 3-dimethylaminopropylamine for 1 hour at 80°-93° C. The reaction product is purified as described in Example 1 to yield 109.9 g (73.2% of theory) of the desired aspartic acid derivative having a melting point of 150°-152.5° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04326069 |
| 出典データセット | uspto-grants-1982_04 |
| ORD ID | ord-ce5aed9be49442b2a92ce4197b18d601 |
| 出典メモ | uspto-grants-1982_04 |