関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Picolyl chloride hydrochloride | HCID 23392 | — |
| 反応物 | 2-Thiohydantoin | HCID 1274030 | — |
| 反応物 | Sodium Methoxide | HCID 10942334 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | HCID 178418295 | HCID 178418295 | — |
反応手順
Initially, 1 g of 2-thiohydantoin and 2.5 g of sodium methylate were dissolved in 50 mL of methanol (MeoH), and 1.5 g of 2-chloromethylpyridine hydrochloride was added to the solution. The reaction mixture was stirred under reflux for one and a half hour and concentrated in vacuo. To the residue, there was added 50 mL of chloroform (CHCl3), and the mixture was washed with 50 mL of water. Then, the CHCL3 layer was dried over magnesium sulfate (MgSO4) and concentrated in vacuo. The residue was purified by column chromatography [using a developing solvent consisting of CHCl3 :MeOH=50:1 (volume ratio, v/v)]. Recrystallization from diethylether gave the desired compound in the form of a needle-like crystal. The yield of this compound was 1.2 g with a yield ratio of 67.2%, and its melting point was 105°-107° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05733922 |
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| 出典データセット | uspto-grants-1998_03 |
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| ORD ID | ord-ee329cf9c57341ee87f8398d0e4b9f66 |
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| 出典メモ | uspto-grants-1998_03 |
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