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HRID 1582970作成日:2026年10月25日

2-Bromothiophene → 2-Chloro-6-methyl-3-(thiophene-2-carbonyl)pyridine

https://huagongshe.com/reaction/1582970

反応式

関与物質

役割名称HCID仕込み量
反応物2-BromothiopheneHCID 13851—
反応物2-Chloro-6-methylnicotinic acidHCID 121724—
反応物MagnesiumHCID 5462224—
溶媒Diethyl EtherHCID 3283—
生成物2-Chloro-6-methyl-3-(thiophene-2-carbonyl)pyridineHCID 22716701—

反応条件

温度0 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06740662B1
出典データセットuspto-grants-2004_05
ORD IDord-d17391885b51489b9a6a73be0ee66e39
出典メモuspto-grants-2004_05