関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Bromothiophene | HCID 13851 | — |
| 反応物 | 2-Chloro-6-methylnicotinic acid | HCID 121724 | — |
| 反応物 | Magnesium | HCID 5462224 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 2-Chloro-6-methyl-3-(thiophene-2-carbonyl)pyridine | HCID 22716701 | — |
反応手順
To a diethyl ether suspension of magnesium was added dropwise 2-bromothiophene at room temperature, and the whole was reacted. After cooling to 0° C., the reaction mixture was added with 2-chloro-6-methylnicotinic acid and, after being warmed to room temperature, the whole was stirred for 12 hours. Thereafter, the reaction mixture was worked up and purified in a usual manner to obtain 2-chloro-6-methyl-3-(thiophene-2-carbonyl)pyridine. NMR1: 7.79 (1H, dd, J=5.0, 1.1 Hz), 7.78 (1H, d, J=7.7 Hz), 2.63 (3H, s).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06740662B1 |
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| 出典データセット | uspto-grants-2004_05 |
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| ORD ID | ord-d17391885b51489b9a6a73be0ee66e39 |
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| 出典メモ | uspto-grants-2004_05 |
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