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Thionyl Chloride → 5-Chloromethyl-2-(2-phenyl-4-thiazolylmethoxy)pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 反応物 | 2-(2-Phenyl-4-thiazolylmethoxy)-5-pyridylmethanol | HCID 22930741 | — |
| 生成物 | 5-Chloromethyl-2-(2-phenyl-4-thiazolylmethoxy)pyridine | HCID 22930783 | 76% |
反応手順
A mixture of 6-(2-phenyl-4-thiazolylmethoxy)-3-pyridylmethanol (2.98 g) and thionyl chloride (15 ml) was stirred at room temperature for 1 hour. The reaction mixture was concentrated under reduced pressure, and saturated aqueous sodium bicarbonate solution was added to the residue, which was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography to obtain 5-chloromethyl-2-(2-phenyl-4-thiazolylmethoxy)pyridine (2.40 g, yield 76%) as colorless crystals from the fraction eluted with ethyl acetate. This was recrystallized from tetrahydrofuran-hexane. Melting point: 117–118° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07179823B1 |
| 出典データセット | uspto-grants-2007_02 |
| ORD ID | ord-246dea5476394e2fb4a32963b4c8066e |
| 出典メモ | uspto-grants-2007_02 |