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3-amino-5-methyl-1H-pyrazole-4-carbonitrile → 2,6-Dimethyl-7-(3-pyridyl)pyrazolo[1,5-a]pyrimidine-3-carbonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-amino-5-methyl-1H-pyrazole-4-carbonitrile | HCID 227460 | — |
| 反応物 | 3-Dimethylamino-2-methyl-1-(3-pyridyl)-2-propen-1-one | HCID 54356480 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | 2,6-Dimethyl-7-(3-pyridyl)pyrazolo[1,5-a]pyrimidine-3-carbonitrile | HCID 11817533 | — |
反応手順
A mixture of 1.90 g. of 3-dimethylamino-2-methyl-1-(3-pyridyl)-2-propen-1-one and 1.22 g. of 3-amino-5-methylpyrazole-4-carbonitrile in 25 ml. of glacial acetic acid is refluxed for 6 hours. The solvent is removed in vacuo and the residue partitioned between dichloromethane and saturated sodium bicarbonate solution. The dichloromethane layer is separated, dried over anhydrous sodium sulfate and passed through a column of hydrous magnesium silicate. The eluent is concentrated and hexane added to give 0.95 g. of the product of the example, m.p. 207°-209° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04281000 |
| 出典データセット | uspto-grants-1981_07 |
| ORD ID | ord-8164944684734bd5a5356bb8e83c1ee0 |
| 出典メモ | uspto-grants-1981_07 |