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3-(4-Phenylpiperazin-1-yl)propan-1-amine → Methyl 3-(1-diphenylmethylpiperazin-4-ylpropylureido)-isovalerate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-(4-Phenylpiperazin-1-yl)propan-1-amine | HCID 261297 | — |
| 反応物 | 3-(4-Benzhydryl-1-piperazinyl)-1-propanamine | HCID 13767778 | — |
| 反応物 | Methyl 3-isocyanato-3-methylbutanoate | HCID 15042553 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | Methyl 3-(1-diphenylmethylpiperazin-4-ylpropylureido)-isovalerate | HCID 70587116 | — |
反応手順
9.0 g (0.029 mol) of 1-diphenylmethyl-4-(3-aminopropyl)-piperazine are dissolved in 30 ml of toluene and according to process alternative (a) mixed with stirring with a mixture of 4.6 g (0.029 mol) of methyl 3-isocyanatoisovalerate and 20 ml of toluene. The mixture is heated for 30 minutes to approximately 70° C., evaporated to dryness under reduced pressure and the oily residue rubbed after the addition of diethyl ether. The methyl 3-(1-diphenylmethylpiperazin-4-ylpropylureido)-isovalerate thus obtained is pure according to its thin-layer chromatogram. ##STR20## Yield: 9.8 g (72% of theory).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04216216 |
| 出典データセット | uspto-grants-1980_08 |
| ORD ID | ord-ae1d5e2c509c4b00829e0d933bec1b77 |
| 出典メモ | uspto-grants-1980_08 |