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HRID 1927602作成日:2026年10月26日

2-Ethylbutyryl chloride → 2-Ethyl-N-{1-[4-(2-ethyl-butyrylamino)-2-fluoro-phenyl]-piperidin-4-yl}-N-phenyl-butyramide

https://huagongshe.com/reaction/1927602

反応式

関与物質

役割名称HCID仕込み量
反応物2-Ethylbutyryl chlorideHCID 75954—
反応物N-[1-(4-amino-2-fluoro-phenyl)-piperidin-4-yl]-2-ethyl-N-phenyl-butyramideHCID 69305096—
溶媒DichloromethaneHCID 6344—
生成物2-Ethyl-N-{1-[4-(2-ethyl-butyrylamino)-2-fluoro-phenyl]-piperidin-4-yl}-N-phenyl-butyramideHCID 1666723231.1%

反応手順

To a mixture of N-[1-(4-amino-2-fluoro-phenyl)-piperidin-4-yl]-2-ethyl-N-phenyl-butyramide (0.30 mmol) and TEA (2.0 mmol) in DCM (10 mL) was added 2-ethyl-butyryl chloride (1.0 mmol). After 16 h, the mixture was washed with H2O (10 mL). The organic layer was concentrated and the residue was purified by PTLC to provide the title compound (45 mg, 31%). MS (ESI): mass calcd. for C29H40FN3O2, 481.31. m/z found, 482.4 [M+H]+. 1H NMR (CDCl3): 7.50-7.35 (m, 5H), 7.15-7.03 (m, 2H), 6.86 (t, J=8.8, 1H), 4.90-4.72 (m, 1H), 3.44-3.30 (m, 2H), 2.80-2.67 (m, 2H), 2.30-1.30 (m, 14H), 0.95 (t, J=7.3, 6H), 0.80 (t, J=7.2, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08183239B2
出典データセットuspto-grants-2012_05
ORD IDord-9e3d8683b99f4ee499cb92dd3c979491
出典メモuspto-grants-2012_05