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1-Phenylpiperazine → 1-(N-Benzyloxycarbonyltyrosyl)-4-phenylpiperazine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-Phenylpiperazine | HCID 7096 | — |
| 反応物 | Dicyclohexylcarbodiimide | HCID 10868 | — |
| 反応物 | N-benzyloxycarbonyl-l-tyrosine | HCID 712438 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 1-(N-Benzyloxycarbonyltyrosyl)-4-phenylpiperazine | HCID 54463856 | 58.6% |
反応手順
12.3 g of N-benzyloxycarbonyltyrosine and 6.6 g of N-phenylpiperazine were dissolved in 150 ml of methylene chloride, and to the solution was added 8.4 g of DCC, and the mixture was stirred at a room temperature for 5 hours. Precipitated insoluble matter was filtered off and the filtrate was concentrated under a reduced pressure, and resulting residue was applied to a silica gel column and eluted with hexane/ethyl acetate (1:1 to 1:2) to obtain 10.5 g of the title compound in a colorless amorphous form.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05245034 |
| 出典データセット | uspto-grants-1993_09 |
| ORD ID | ord-6fb0cb4113fb499eb4dfc30867774f34 |
| 出典メモ | uspto-grants-1993_09 |