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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 2-(2-phenyl-4-thiazolylmethoxy)-5-pyridylmethanol (2.98 g) and thionyl chloride (15 ml) was stirred at room temperature for 1 hr. The reaction mixture was concentrated under reduced pressure and saturated aqueous sodium hydrogen carbonate was added to the residue. The mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography, and 5-chloromethyl-2-(2-phenyl-4-thiazolylmethoxy)pyridine (2.40 g, yield 76%) was obtained as colorless crystals from a fraction eluted with ethyl acetate. The crystals were 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 | US07241785B2 |
| 出典データセット | uspto-grants-2007_07 |
| ORD ID | ord-6f58bfa0c4e14e6794e161c66fccea0a |
| 出典メモ | uspto-grants-2007_07 |