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HRID 19472作成日:2026年10月25日

1-Methylpiperazine → 1-(4-Bromo-2-methylbenzoyl)-4-methylpiperazine

https://huagongshe.com/reaction/19472

反応式

関与物質

役割名称HCID仕込み量
反応物1-MethylpiperazineHCID 53167—
反応物DiisopropylethylamineHCID 81531—
反応物4-Bromo-2-methylbenzoic acidHCID 99570—
反応物Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
溶媒DimethylformamideHCID 6228—
生成物1-(4-Bromo-2-methylbenzoyl)-4-methylpiperazineHCID 59392754—

反応手順

4-Bromo-2-methylbenzoic acid (10 g, 46.5 mmol), and HBTU (23 g, 60.5 mmol) were dissolved in DMF (150 mL), then N-methyl piperazine (6.0 g, 60.5 mmol) and DIPEA (21 mL, 121 mmol) were added. The reaction was stirred overnight before the removal of the DMF in vacuo, the gum was quenched with 2.0N NaOH (100 mL), extracted with diethyl ether (3×200 mL), dried (MgSO4) and solvent removed in vacuo to yield a viscous gum. Purification on silica using 0-10% MeOH in DCM as eluent, gave the title compound as viscous oil. The oil was dissolved in the minimum amount of diethyl ether, iso-hexane was added to give a colourless solid which was filtered and dried (11.8 g, 86%); 1H NMR (CDCl3) 7.40 (s, 1H), 7.36 (d, 1H), 7.04 (d, 1H), 3.86-3.79 (m, 2H), 3.27-3.21 (m, 2H), 2.51-2.45 (m, 2H), 2.32-2.29 (m, 8H); MH+ 298.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745428B2
出典データセットuspto-grants-2010_06
ORD IDord-737e58edd27a47cbba07fbab19ebb2d9
出典メモuspto-grants-2010_06