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Methane → (2S)-2-[[(2S)-1-ethoxy-1-oxopentan-2-yl]amino]propanoic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methane | HCID 297 | — |
| 反応物 | N-[(S)-1-Carbethoxybutyl]-(S)-alanine Benzyl Ester | HCID 11493275 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | (2S)-2-[[(2S)-1-ethoxy-1-oxopentan-2-yl]amino]propanoic acid | HCID 10015159 | 59.5% |
反応手順
A solution of N-[1-(S)-ethoxycarbonyl-1-butyl]-(S)-alanine benzyl ester (14.5 g, as obtained in Step-I) in ethanol (150 ml) was hydrogenated in the presence of 10% palladised charcoal (0.8 g) under 40-45 psi hydrogen pressure for 1.5 to 2 hrs. The reaction mixture was concentrated under reduced pressure to give an oil. Crystallization from a mixture of acetonitrile and ethanol (1:3) gave 6.1 g the title compound
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07456296B2 |
| 出典データセット | uspto-grants-2008_11 |
| ORD ID | ord-a9b05529552d4269b5cbb7a76c665f81 |
| 出典メモ | uspto-grants-2008_11 |