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Dicyclohexylcarbodiimide → Urea
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dicyclohexylcarbodiimide | HCID 10868 | — |
| 反応物 | Aminopterin | HCID 169371 | — |
| 反応物 | Leu-Ala-Leu-Ala | HCID 53729605 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | Urea | HCID 1176 | — |
| 生成物 | Aminopterin | HCID 169371 | — |
反応手順
Conjugation Via Leu-Ala-Leu-Ala Spacer: The N-hydroxysuccinimide ester of aminopterin was prepared as above. To 10.2 ml of a 23 mM solution of the aminopterin derivative (0,236 mmol) in dimethylformamide were added 104 mg (0,236 mmol) of solid L-Leu-L-Ala-L-Leu-L-Ala (LALA). The mixture was stirred overnight at 50° C. during which time the solid LALA dissolved. To the reaction mixture was added 48.7 mg (0.236 mmol) of dicyclohexylcarbodiimide in 0.58 ml of dimethylformamide. Copious quantities of urea formed within 2 hours at room temperature and were removed by filtration. The filtrate containing the N-hydroxy succinimide ester of the LALA derivative of aminopterin was retained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05474765 |
| 出典データセット | uspto-grants-1995_12 |
| ORD ID | ord-54fbf15dbc4e4b49a3124476191332a0 |
| 出典メモ | uspto-grants-1995_12 |