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Hydrochloric Acid → (E)-2-(2,4-Difluorostyryl)-1-(2-pyridyl)-1H-benzimidazole hydrochloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | N1-(pyridin-2-yl)benzene-1,2-diamine | HCID 752150 | — |
| 反応物 | (E)-1-(2-pyridyl)-2-styryl-1H-benzimidazole | HCID 9796241 | — |
| 反応物 | HCID 11159992 | HCID 11159992 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | (E)-2-(2,4-Difluorostyryl)-1-(2-pyridyl)-1H-benzimidazole hydrochloride | HCID 22736765 | — |
反応手順
To a solution of (E)-2,4-difluorocinnamic acid (331 mg, 1.8 mmol) in benzene (10 ml) was added thionyl chloride (0.5 ml) and the mixture was heated to reflux for 60 min. Volatiles were removed by evaporation to give crude (E)-2,4-difluorocinnamoyl chloride. Free base of the titled compound was prepared from N-(2-pyridyl)-o-phenylenediamine (250 mg, 1.4 mmol) and (E)-2,4-difluorocinnamoyl chloride obtained as above according to the preparation of (E)-1-(2-pyridyl)-2-styryl-1H-benzimidazole (Example 1, method A). The free base was dissolved with a 10% methanol solution of hydrogen chloride (5 ml). Concentration and recrystallization from ethyl acetate/ethanol yielded the titled compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06310079B1 |
| 出典データセット | uspto-grants-2001_10 |
| ORD ID | ord-9429f9f5a3234f3b82015b3f235885a4 |
| 出典メモ | uspto-grants-2001_10 |