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[1-(2-Azidoethyl)-2-(phenylmethylene)hydrazino]oxoacetic acid, ethyl ester → 1-(Benzylideneamino)piperazine-2,3-dione
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | [1-(2-Azidoethyl)-2-(phenylmethylene)hydrazino]oxoacetic acid, ethyl ester | HCID 86736838 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 触媒 | Lindlars catalyst | HCID 131709914 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 1-(Benzylideneamino)piperazine-2,3-dione | HCID 53848040 | — |
反応手順
2 g. of the ethyl ester product from part (d) are dissolved in 100 ml. of ethanol. 0.5 g. of Lindlar catalyst are added and the reaction mixture is stirred for four hours at room temperature under two atmospheres of hydrogen. At intervals the reaction mixture is filtered. After completion of the slow absorption of hydrogen, the reaction solution is flooded with nitrogen and then heated to a boil. This mixture is filtered while hot and after cooling 1 g. of crude product is obtained from the filtrate. Recrystallization from water yields as white crystals purified 1-[(phenylmethylene)amino]-2,3-piperazinedione; m.p. 229°-231°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04386199 |
| 出典データセット | uspto-grants-1983_05 |
| ORD ID | ord-bf4ee007285d4286a35da233d27efc0f |
| 出典メモ | uspto-grants-1983_05 |