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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 415311생성일: 2026년 10월 25일

1-Hydroxybenzotriazole → Methyl 3-(4-isobutyrylpiperazine-1-carbonyl)benzoate

https://huagongshe.com/reaction/415311

반응식

참여 물질

역할이름HCID투입량
반응물1-HydroxybenzotriazoleHCID 75771—
반응물3-(Methoxycarbonyl)benzoic acidHCID 601880—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물2-Methyl-1-(piperazin-1-yl)propan-1-oneHCID 2761409—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물Methyl 3-(4-isobutyrylpiperazine-1-carbonyl)benzoateHCID 6662131494%

반응 단계

To a solution of 3-(methoxycarbonyl)benzoic acid (0.9 g, 5 mmol) in dichloromethane (20 mL), 1-hydroxybenzotriazole (0.75 g, 5.5 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (1.06 g, 5.5 mmol) and triethyl amine (2 mL) was added. The mixture was stirred at room temperature for 30 min, then 2-methyl-1-(piperazin-1-yl)propan-1-one (1.0 g, 5 mmol) was added and the mixture was stirred at room temperature for 16 h. The resulting mixture was added water (50 mL) and extracted with dichloromethane (100 mL×3). The organic phase was washed with sodium bicarbonate and brine and concentrated. The crude product was purified by column chromatography (silica gel, petroleum ether/ethyl acetate 20:1 to 2:1) to give 1.25 g of methyl 3-(4-isobutyrylpiperazine-1-carbonyl)benzoate as an oil. Yield 94%. 1H-NMR (400 MHz, CDCl3) 1.14-1.15 (d, J=6.4 Hz, 6H), 2.81 (brs, 1H), 3.44-3.80 (m, 8H), 3.94 (s, 3H), 7.52-7.55 (t, J=7.6 Hz, 1H), 7.62-7.64 (d, J=8.0 Hz, 1H), 8.08-8.14 (m, 2H); LC-MS (ESI) m/z: 319 (M+1)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08088760B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-381c6ffd2c4447ddb5ac0084cb7cdfed
출처 메모uspto-grants-2012_01