関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dicyclohexylcarbodiimide | HCID 10868 | — |
| 反応物 | Fmoc-L-Asp(OtBu)-OH | HCID 2724635 | — |
| 反応物 | L-tryptophan benzyl ester hydrochloride | HCID 45073232 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Fmoc-L-aspartic acid | HCID 7019016 | 189.2% |
反応手順
41 mg of Fmoc-Asp(Ot-Bu)-OH was dissolved in 1 ml of methylene chloride. The solution was cooled to 0° C., and then 12 mg of HONSu and 21 mg of DCC were added thereto. The mixture was stirred at 0° C. for 30 minutes. To the mixture were added 1 ml of a methylene chloride containing 33 mg of H-Trp-OBzl.HCl and 14 μl of TEA, followed by stirring,at 0° C. for 3 hours. The insoluble matters were filtered off and the filtrate was washed with cold methylene chloride. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (Wakogel C-200, manufactured by Wako Junyaku Kogyo, 50 g, elution with chloroform/methanol=25/1), to obtain 67 mg of Fmoc-Asp(Ot-Bu-Trp-OBz1 as a white powder.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05639860 |
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| 出典データセット | uspto-grants-1997_06 |
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| ORD ID | ord-0d7f38f7d52b45cdbc2e55c54874464a |
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| 出典メモ | uspto-grants-1997_06 |
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