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Sodium 4-methyl-2-oxovalerate → N-(1-Carboxy-3-methylbutyl)-L-alanyl-L-isoleucine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium 4-methyl-2-oxovalerate | HCID 4137900 | — |
| 反応物 | Sodium cyanoborohydride | HCID 5003444 | — |
| 反応物 | Ala-Ile | HCID 7408079 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | N-(1-Carboxy-3-methylbutyl)-L-alanyl-L-isoleucine | HCID 53653027 | 85.2% |
反応手順
A solution of L-alanyl-L-isoleucine (150 mg) and 4-methyl-2-oxopentanoic acid sodium salt (564 mg) in water was adjusted to pH 7 and treated with 140 mg of sodium cyanoborohydride at room temperature for several days. The reaction was quenched with strong acid ion-exchange resin, added to a column of the same resin, and eluted with 2% pyridine in water. Freeze drying afforded 200 mg (84.9%) of white fluffy solid, N-(1-carboxy-3-methylbutyl)-L-alanyl-L-isoleucine. Mass spectrum showed peaks at 460 for the disilylated derivative, and 445 for disilyl molecular ion minus methyl (460-15). The nmr spectrum showed a broad doublet centered at 0.95 ppm, complex absorption in the 1.2-1.8 ppm range, and a broad weak singlet at 3.7 ppm.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04374829 |
| 出典データセット | uspto-grants-1983_02 |
| ORD ID | ord-ea3cb8a871d64c27860694e436ac4ae7 |
| 出典メモ | uspto-grants-1983_02 |