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HRID 749441作成日:2026年10月25日

Methylamine → 2-(4-fluorophenyl)-N-methylpent-4-enamide

https://huagongshe.com/reaction/749441

反応式

関与物質

役割名称HCID仕込み量
反応物MethylamineHCID 6329—
反応物DiisopropylethylamineHCID 81531—
反応物O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
反応物2-(4-Fluorophenyl)pent-4-enoic acidHCID 18354511—
溶媒DichloromethaneHCID 6344—
生成物2-(4-fluorophenyl)-N-methylpent-4-enamideHCID 6897726178.2%

反応手順

2-(4-Fluorophenyl)pent-4-enoic acid (Bioorg. Med. Chem. Lett. 2000, 1893; 4.20 g, 21.6 mmol) was dissolved in CH2Cl2 (75 mL) and to the resultant solution was added TBTU (7.29 g, 22.7 mmol). The mixture was stirred at RT for 15 min and then methylamine (11.9 mL of 2M THF solution, 23.8 mmol) and DIPEA (11.2 g, 86.5 mmol) were added. The reaction mixture was stirred at room temperature for 3 h, subsequently diluted with CH2Cl2 (50 mL) and then washed several times with water. The solvent was removed by evaporation and the residue flash chromatographed on silica gel (heptane-ethyl acetate, 1:1). There was obtained 3.5 g (78%) of 2-(4-fluorophenyl)-N-methylpent-4-enamide as an oil, which shortly after crystallized. 1H NMR (400 MHz, CDCl3): 2.5 (qn, 1H), 2.7 (d, 3H), 2.9 (qn, 1H), 3.4 (t, 1H), 4.9-5.1 (m, 2H), 5.6-5.8 (m, 1H), 6.0-6.2 (b, 1H), 7.0 (m, 2H), 7.3 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07402581B2
出典データセットuspto-grants-2008_07
ORD IDord-007169fc74734a77aee59a9efc90c533
出典メモuspto-grants-2008_07