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Malononitrile → 2-Amino-4-(4-cyanophenyl)-6-methyl-1-[3-(trifluoromethyl)phenyl]-1,4-dihydro-3,5-pyridinedicarbonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Malononitrile | HCID 8010 | — |
| 反応物 | Piperidine | HCID 8082 | — |
| 反応物 | 4-Cyanobenzaldehyde | HCID 66042 | — |
| 反応物 | 3-{[3-(Trifluoromethyl)phenyl]amino}but-2-enenitrile | HCID 5075287 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 2-Amino-4-(4-cyanophenyl)-6-methyl-1-[3-(trifluoromethyl)phenyl]-1,4-dihydro-3,5-pyridinedicarbonitrile | HCID 68425782 | — |
反応手順
Under argon, 750 mg (3.32 mmol) of the compound of Example 2A, 434.79 mg (3.32 mmol) 4-formylbenzonitrile and 219.04 mg (3.32 mmol) malononitrile are dissolved in 5 ml ethanol. 28.23 mg (33 μl, 0.33 mmol) piperidine are added, and the mixture is stirred at reflux overnight. The product is crystallised from the reaction mixture at 0° C. The formed crystals are filtered, washed twice with cold ethanol and dried.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07691854B2 |
| 出典データセット | uspto-grants-2010_04 |
| ORD ID | ord-55295e84040343069f77af3aef68c500 |
| 出典メモ | uspto-grants-2010_04 |