関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Methylmorpholine | HCID 7972 | — |
| 反応物 | HCID 13273165 | HCID 13273165 | — |
| 反応物 | Benzyl glycyl-L-alaninate hydrochloride | HCID 53328828 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-t-butoxycarbonyl-L-tyrosylglycyl-L-alanine benzyl ester | HCID 53750798 | — |
反応手順
A solution of 17.6 parts N-t-butoxycarbonyl-L-tyrosine 2,4,5-trichlorophenyl ester, 9.0 parts glycyl-L-alanine benzyl ester hydrochloride and 1.2 parts N-methylmorpholine in 200 parts methylene chloride is stirred for 16 hours at room temperature. Removal of the solvent under reduced pressure affords a crude product which is purified by low pressure column chromatography to give N-t-butoxycarbonyl-L-tyrosylglycyl-L-alanine benzyl ester. The purified material is dissolved in 400 parts methanol. Then, 0.4 part palladium black metal catalyst is added and the mixture shaken with hydrogen at atmospheric pressure and room temperature for about 5 hours. The catalyst is removed by filtration, and the solvent is removed by evaporation under reduced pressure. The resulting material is purified by low-pressure chromatography to give N-t-butoxycarbonyl-L-tyrosylglycyl-L-alanine. This compound is represented by the following formula
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04028319 |
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| 出典データセット | uspto-grants-1977_06 |
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| ORD ID | ord-7dd09a1cefae4b53a49903cf89014486 |
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| 出典メモ | uspto-grants-1977_06 |
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