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Diethyl Ether → 5-Amino-1-(2,6-dimethylphenyl)-1H-pyrazole-4-carbonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diethyl Ether | HCID 3283 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 2-(Ethoxymethylene)propanedinitrile | HCID 67152 | — |
| 反応物 | 2,6-Dimethylphenylhydrazine hydrochloride | HCID 12405010 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 5-Amino-1-(2,6-dimethylphenyl)-1H-pyrazole-4-carbonitrile | HCID 12150554 | — |
反応手順
3.0 g (17.3 mmol) of 2,6-dimethylphenylhydrazine hydrochloride are suspended with 2.1 g (17.3 mmol) of ethoxymethylenemalononitrile in 40 ml of ethanol, and 7.3 ml (52.1 mmol) of triethylamine are added. The reaction mixture is heated to reflux for 3 h, during which a clear solution forms. After cooling to room temperature, diethyl ether is added to this. The triethylammonium chloride which precipitates is filtered off. The solvent is removed in vacuo, and the residue is purified by preparative HPLC (YMC gel ODS-AQ S 5/15 μm; eluent A: water, eluent B: acetonitrile; gradient: 0 min 30% B, 5 min 30% B, 50 min 95% B). 2.3 g (62% of theory) of the product are obtained as yellow crystals.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08809348B2 |
| 出典データセット | uspto-grants-2014_08 |
| ORD ID | ord-6eee0d69dcc648408a359c26045562e4 |
| 出典メモ | uspto-grants-2014_08 |