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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19472생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/19472

반응식

참여 물질

역할이름HCID투입량
반응물1-MethylpiperazineHCID 53167—
반응물DiisopropylethylamineHCID 81531—
반응물4-Bromo-2-methylbenzoic acidHCID 99570—
반응물Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
용매DimethylformamideHCID 6228—
생성물1-(4-Bromo-2-methylbenzoyl)-4-methylpiperazineHCID 59392754—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745428B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-737e58edd27a47cbba07fbab19ebb2d9
출처 메모uspto-grants-2010_06