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4-Amino-2,6-dimethylphenol → 2,6-dimethyl-4-[(2-phenyl-3,4-dihydropyrazol-5-yl)amino]phenol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Amino-2,6-dimethylphenol | HCID 82668 | — |
| 反応物 | 3-Amino-1-phenylpyrazole | HCID 98736 | — |
| 触媒 | p-Toluenesulfonic acid | HCID 6101 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2,6-dimethyl-4-[(2-phenyl-3,4-dihydropyrazol-5-yl)amino]phenol | HCID 178428364 | 46.2% |
反応手順
2,6-dimethyl-4-aminophenol (15 g) and 4,5-dihydro-1-phenyl-1H-pyrazol-3-amine (17.6 g) were heated with p-toluene sulfonic acid (0.2 g) at 160° for 1 hour under nitrogen. The mix was cooled, taken up in dichloromethane and washed with dilute HCl, and water. Evaporation, and chromatography of the residue (silica, dichloromethane/ethyl acetate [9:1]) gave 4-(4,5-dihydro-1-phenyl-1H-pyrazol-3-yl)amino-2,6-dimethylphenol (14.2 g), mp 154°-158°. This was refluxed in toluene (40 ml) with 10% palladium on charcoal (10 g) for 3 hours. The mixture was filtered and evaporated to give, after crystallisation from cyclohexane/ethyl acetate, the title compound (8 g), mp 154°-155°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05428044 |
| 出典データセット | uspto-grants-1995_06 |
| ORD ID | ord-588e7610c0864434bdfdba69889f02e0 |
| 出典メモ | uspto-grants-1995_06 |