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HRID 449930作成日:2026年10月25日

2,6-Dichlorobenzoyl chloride → N-(3-fluoropyridin-4-yl)-2,6-dichlorobenzamide

https://huagongshe.com/reaction/449930

反応式

関与物質

役割名称HCID仕込み量
反応物2,6-Dichlorobenzoyl chlorideHCID 78392—
反応物DiisopropylethylamineHCID 81531—
反応物4-Amino-3-fluoropyridineHCID 817122—
溶媒AcetonitrileHCID 6342—
溶媒DichloromethaneHCID 6344—
生成物N-(3-fluoropyridin-4-yl)-2,6-dichlorobenzamideHCID 5961808047.3%

反応手順

To a cooled (0° C.) mixture of 3-fluoropyridin-4-amine (1.0 g, 8.9 mmol) and DIPEA (2.7 mL, 18 mmol) in dichloromethane (20 mL) and MeCN (10 mL) was added a solution of 2,6-dichlorobenzoyl chloride (2.1 g, 9.8 mmol) in dichloromethane (20 mL). The reaction mixture was stirred at room temperature overnight and concentrated under reduced pressure. The residue was partitioned between EtOAc (30 mL) and sat. NaHCO3 (30 mL). The aqueous layer was extracted with EtOAc (2×15 mL) and then the combined organic extracts were concentrated under reduced pressure. The residue was purified by silica gel column chromatography (EtOAc) to afford N-(3-fluoropyridin-4-yl)-2,6-dichlorobenzamide (1.2 g, yield: 47%). 1H NMR (400 MHz, DMSO) δ 11.21 (s, 1H), 8.59 (d, J=2.8, 1H), 8.41 (d, J=5.4, 1H), 8.21 (dd, J=6.7, 5.4, 1H), 7.77-7.33 (m, 3H). LCMS (ESI) m/z: 285.2 [M+H+]

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08486950B2
出典データセットuspto-grants-2013_07
ORD IDord-ac4191c165004976b2b536ab8378f3fd
出典メモuspto-grants-2013_07