関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Propargyl bromide | HCID 7842 | — |
| 反応物 | Hexane | HCID 8058 | — |
| 反応物 | N-Methylbenzothiazol-2-amine | HCID 28160 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-(N-methyl-N-propynylamino)benzothiazole | HCID 20271333 | 84% |
反応手順
2-Methylaminobenzothiazole (c) (14.0 g) was dissolved in anhydrous tetrahydrofuran (250 ml) and a hexane solution (73 ml) of butyl lithium (6.53 g) was added thereto at -78° C. with stirring. The mixture was stirred for 1.5 hours under cooling and 2-propynyl bromide (8.4 ml) was dropwise added thereto. The resultant mixture was allowed to stand at room temperature overnight and then evaporated to remove the solvent. After addition of water, the residue was extracted with ether. The extract was washed with water, dried and evaporated to remove the solvent. The resultant residue was applied to column chromatography on silica gel (280 g) to give 2-(N-methyl-N-propynylamino)benzothiazole (d) (14.5 g, yield 84%) from chloroform eluate.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04535088 |
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| 出典データセット | uspto-grants-1985_08 |
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| ORD ID | ord-655eb8d90eae40d1a7ee035d7ffa7030 |
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| 出典メモ | uspto-grants-1985_08 |
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