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Triethylamine → (3-(2-Pyridyldithio)propionyl) (6-aminohexoxvhydroxy-phosphinyl)oxy-N,N,N-trimethylethanaminium hydroxide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | N-Succinimidyl 3-(2-pyridyldithio)propionate | HCID 100682 | — |
| 反応物 | HCID 88407369 | HCID 88407369 | — |
| 溶媒 | Dimethyl Sulfoxide | HCID 679 | — |
| 生成物 | (3-(2-Pyridyldithio)propionyl) (6-aminohexoxvhydroxy-phosphinyl)oxy-N,N,N-trimethylethanaminium hydroxide | HCID 131719547 | — |
反応手順
2-[(6-Aminohexoxyhydroxyphosphinyl)oxy-N,N,N-trimethylethanaminium hydroxide, inner salt (90 mg, 0.28 mmol) was dissolved in dry dimethyl sulphoxide (2 ml). Triethylamine (197 μl, 1.41 mmol) was added, followed by N-succinimidyl 3-(2-pyridyldithio)propionate (88 mg, 0.28 mmol). The mixture was stirred at ambient temperature for eighteen hours. The solvent was evaporated under vacuum at a temperature of 60° C. and re-evaporated from methanol. The residue was chromatographed on silica gel eluting with methanol. The relevant fractions were combined and evaporated to dryness to give 2[N(3-(2 pyridyldithio)propionyl)(6-aminohexoxyhydroxy
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05556710 |
| 出典データセット | uspto-grants-1996_09 |
| ORD ID | ord-3a475cbe09e944b69e8e34e4f420c6a0 |
| 出典メモ | uspto-grants-1996_09 |