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HRID 1892755作成日:2026年10月25日

Methyl 6-formylpyridine-3-carboxylate → methyl 6-((5-methyl-6-(4-(trifluoromethyl)-1H-pyrazol-1-yl)pyridin-3-ylimino)methyl)nicotinate

https://huagongshe.com/reaction/1892755

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 6-formylpyridine-3-carboxylateHCID 586269—
反応物5-methyl-6-(4-(trifluoromethyl)-1H-pyrazol-1-yl)pyridin-3-amineHCID 64173725—
溶媒TolueneHCID 1140—
生成物methyl 6-((5-methyl-6-(4-(trifluoromethyl)-1H-pyrazol-1-yl)pyridin-3-ylimino)methyl)nicotinateHCID 68156512100%

反応手順

A mixture of methyl 6-formylnicotinate (251.3 mg, 1.52 mmol) and 5-methyl-6-(4-(trifluoromethyl)-1H-pyrazol-1-yl)pyridin-3-amine (369 mg, 1.52 mmol) in toluene (8 mL) was heated at reflux under nitrogen overnight. The reaction mixture was concentrated to give methyl 6-((5-methyl-6-(4-(trifluoromethyl)-1H-pyrazol-1-yl)pyridin-3-ylimino)methyl)nicotinate (592 mg, 100%). 1H NMR (400 MHz, (CD3)2SO, δ): 9.09 (d, 1H), 8.83 (s, 1H), 8.72 (s, 1H), 8.35-8.30 (m, 2H), 8.20-8.17 (m, 1H), 8.11 (s, 1H), 7.90 (d, 1H), 3.79 (s, 3H), 2.32 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08507533B2
出典データセットuspto-grants-2013_08
ORD IDord-21f06cfba8d7447084d1fe920bf6e120
出典メモuspto-grants-2013_08