戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 228174作成日:2026年10月26日

Benzoyl chloride → 6-[4-(2-Benzoylamino-ethyl)-phenoxy]-nicotinamide

https://huagongshe.com/reaction/228174

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoyl chlorideHCID 7412—
反応物TriethylamineHCID 8471—
反応物6-[4-(2-Amino-ethyl)-phenoxy]-nicotinamideHCID 59730017—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物6-[4-(2-Benzoylamino-ethyl)-phenoxy]-nicotinamideHCID 59730051—

反応手順

Combine amine starting material of Example 34 (100 mg, 0.39 mmol), benzoyl chloride (50 μL, 0.43 mmol) and Et3N (120 μL, 0.86 mmol) in THF (4 mL) and DMF (0.5 mL). Stir the mixture at room temperature for 3 hours. Eliminate the solvent and purify by flash chromatography on silica gel (eluent: EtOAc/hexane 75/25) to give the title compound. (90 mg, 65%). Electrospray MS M+1 ion=362, 1H-NMR (methanol-d4, 400 MHz): 8.62 (d, 1H, J=2.8 Hz), 8.24 (dd, 1H, J=2.8 and 9.0 Hz), 7.79-7.76 (m, 2H), 7.55-7.42 (m, 5H), 7.09-7.06 (m, 2H), 6.96 (d, 1H, J=9.0 Hz), 3.62 (t, 2H, J=7.3 Hz), 2.95 (t, 2H, J=7.3 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07560463B2
出典データセットuspto-grants-2009_07
ORD IDord-4c8718eb6ac248d58ca33f1a4c5ff275
出典メモuspto-grants-2009_07