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HRID 2212346作成日:2026年10月27日

3-Pyridinecarbonyl chloride, hydrochloride (1:1) → N-[4-(4-Methoxyphenyl)-5-{2-[(pyridine-3-carbonyl)amino]pyridin-4-yl}-1,3-thiazol-2-yl]pyridine-3-carboxamide

https://huagongshe.com/reaction/2212346

反応式

関与物質

役割名称HCID仕込み量
反応物3-Pyridinecarbonyl chloride, hydrochloride (1:1)HCID 88438—
反応物Sodium BicarbonateHCID 516892—
反応物4-[2-Amino-4-(4-methoxyphenyl)-1,3-thiazol-5-yl]-2-pyridylamineHCID 9966038—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DimethylacetamideHCID 31374—
生成物N-[4-(4-Methoxyphenyl)-5-{2-[(pyridine-3-carbonyl)amino]pyridin-4-yl}-1,3-thiazol-2-yl]pyridine-3-carboxamideHCID 987090533%

反応条件

温度70 °C

反応手順

Nicotinoyl chloride hydrochloride (0.72 g, 4.1 mmol) and 4-dimethylaminopyridine (0.05 g, 0.4 mmol) were added to a solution of 4-[2-amino-4-(4-methoxyphenyl)-1,3-thiazol-5-yl]-2-pyridylamine (0.41 g, 1.4 mmol) in N,N-dimethylacetamide (10 mL) and the mixture was stirred at 70° C. for 19 hours. After the reaction mixture was cooled to room temperature, a saturated aqueous solution of sodium hydrogencarbonate (50 mL) was added. The resulting crude crystals were collected by filtration and washed with water. The crude crystals were recrystallized from ethanol to obtain 0.23 g (0.44 mmol, yield 33%) of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07101899B1
出典データセットuspto-grants-2006_09
ORD IDord-97c70ef57e1046a68df529d66d38fed8
出典メモuspto-grants-2006_09