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1-(4-methylbenzyl)-3-nitro-1H-pyrazole → 1-(4-Methylbenzyl)-1H-pyrazol-3-amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-(4-methylbenzyl)-3-nitro-1H-pyrazole | HCID 7010174 | — |
| 触媒 | Nickel | HCID 935 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Hydrazine | HCID 9321 | — |
| 生成物 | 1-(4-Methylbenzyl)-1H-pyrazol-3-amine | HCID 571039 | — |
反応手順
To a solution containing 1-(4-methyl-benzyl)-3-nitro-1H-pyrazole (92 mg, 0.42 mmol) in tetrahydrofuran (2 mL), anhydrous hydrazine (100 μL) was added to the clear solution. Raney nickel (˜100 mg washed 3 times with 5 mL of anhydrous tetrahydrofuran) was then added in tetrahydrofuran (300 μL). Gas evolved from the mixture and the reaction was allowed to proceed for 5 min, after which time the raney nickel was removed by filtration through a celite plug. The solvent was removed in vacuo to afford 1-(4-methyl-benzyl)-1H-pyrazol-3-ylamine as a yellow oil which was used in the following step with no further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07935699B2 |
| 出典データセット | uspto-grants-2011_05 |
| ORD ID | ord-f11207cfe36b4a66a84f0f32ba581c7f |
| 出典メモ | uspto-grants-2011_05 |