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3-Methyl-2-thiophenecarboxaldehyde → (3-Methylthien-2-ylmethyl)-[4-(5-methylthio-3-pyridin-4-yl-1H-1,2,4-triazol-1-yl)phenyl]amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-Methyl-2-thiophenecarboxaldehyde | HCID 79911 | — |
| 反応物 | Sodium cyanoborohydride | HCID 5003444 | — |
| 反応物 | 1-(4-aminophenyl)-5-methylthio-3-(4-pyridyl)-1H-1,2,4-triazole | HCID 18425871 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | (3-Methylthien-2-ylmethyl)-[4-(5-methylthio-3-pyridin-4-yl-1H-1,2,4-triazol-1-yl)phenyl]amine | HCID 18425879 | — |
反応手順
A stirred solution of 1-(4-aminophenyl)-5-methylthio-3-(4-pyridyl)-1H-1,2,4-triazole (Example 1) (100 mg, 0.35 mmol) and 3-methylthiophene-2-carboxaldehyde (44 mg, 0.35 mmol) in 5% acetic acid in MeOH (4 mL) at room temperature was treated with sodium cyanoborohydride (55 mg, 0.88 mmol) and the reaction mixture was further stirred at room temperature for 48 h. The reaction mixture was concentrated, diluted with EtOAc, washed with NaHCO3 solution, brine and dried (MgSO4). The residue obtained on concentration was flash chromatographed on silica gel and eluted with a gradient of dichloromethane/acetone (9/1 to 3/1). The title compound was obtained as a white solid (85 mg).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06451820B1 |
| 出典データセット | uspto-grants-2002_09 |
| ORD ID | ord-34d645a9fa704ad29676d2a9f47237ce |
| 出典メモ | uspto-grants-2002_09 |