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m-Chloroperbenzoic acid → 1-(2-Acetylaminoethyl)-4-methanesulphinylpyridinium chloride
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | m-Chloroperbenzoic acid | HCID 70297 | — |
| 反応物 | N-(2-Chloroethyl)acetamide | HCID 81815 | — |
| 反応物 | 4-(Methylthio)pyridine | HCID 140938 | — |
| 溶媒 | Trifluoroacetic acid methylene chloride | HCID 21863450 | — |
| 生成物 | 1-(2-Acetylaminoethyl)-4-methanesulphinylpyridinium chloride | HCID 20028995 | — |
反応手順
The starting material may be obtained as follows: Reaction of 4-methylthiopyridine with 4 equivalents of N-acetyl-2-chloroethylamine at 80° for 4 hours gave, after precipitation from CH2Cl2 solution with EtOAc, 1-(2-acetylaminoethyl)-4-methylthiopyridinium chloride in solvent B: 1.76(s, 3H); 2.69(s, 3H); 3.6(t, 2H); 4.5(t, 2H); 7.87(d, 2H); 8.64(d, 2H). This compound was reacted with one equivalent of metachlorperbenzoic acid in CH2Cl2 /TFA at 0° to ambient temperature for 30 minutes. The product was precipitated from CH2Cl2 /MeOH solution with ether to give 1-(2-acetylaminoethyl)-4-methanesulphinylpyridinium chloride. n.m.r. in solvent B: 1.76(s, 3H); 3.0(s, 3H); 3.66(t, 2H); 4.74(t, 2H); 8.47(d, 2H); 9.22(d, 2H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04678781 |
| 出典データセット | uspto-grants-1987_07 |
| ORD ID | ord-3f66bd1ffc9c4959a28360153d3e8a72 |
| 出典メモ | uspto-grants-1987_07 |