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Phenylacetyl chloride → N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N-ethyl-N'-(2-phenylacetyl)thiourea
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Phenylacetyl chloride | HCID 7679 | — |
| 反応物 | Phenylacetyl isothiocyanate | HCID 12454157 | — |
| 反応物 | N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N-ethylamine | HCID 21891226 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | Phenylacetyl isothiocyanate | HCID 12454157 | — |
| 生成物 | N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N-ethyl-N'-(2-phenylacetyl)thiourea | HCID 21890890 | 48% |
反応手順
2-Phenylethanoyl isothiocyanate was prepared using commercially available 2-phenylethanoyl chloride (80 mg) as a starting compound according to the description of the literature. N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}-N-ethylamine (50 mg) was dissolved in toluene (5 ml) and ethanol (1 ml) to prepare a solution. A solution of 2-phenylethanoyl isothiocyanate in ethanol (1 ml) was then added to the solution, and the mixture was stirred at room temperature for 2 hr. The reaction solution was concentrated, and the residue was purified by chromatography on silica gel using chloroform/acetone for development to give the title compound (38 mg, yield 48%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07135466B2 |
| 出典データセット | uspto-grants-2006_11 |
| ORD ID | ord-208e0798d67c46f8a3da0f3164ad837b |
| 出典メモ | uspto-grants-2006_11 |