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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16775생성일: 2026년 10월 24일

Pyridine → Methyl 4-(4-methylpiperazine-1-carbonyl)benzoate

https://huagongshe.com/ko/reaction/16775

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Monomethyl terephthalateHCID 15513—
반응물1-MethylpiperazineHCID 53167—
반응물Oxalyl chlorideHCID 65578—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물Methyl 4-(4-methylpiperazine-1-carbonyl)benzoateHCID 1717822367.9%

반응 단계

Oxalyl chloride (0.533 mL, 6.11 mmol) was added dropwise to a stirred suspension of 4-(methoxycarbonyl)benzoic acid (1 g, 5.55 mmol) in DCM (20 mL) under nitrogen. The resulting suspension was stirred at room temperature for 30 mins. DMF (0.05 mL) was added dropwise under nitrogen. The resulting suspension was stirred for 90 mins. A solution of 1-methylpiperazine (0.554 mL, 5.00 mmol) and pyridine (1.211 mL, 14.99 mmol) in DCM (15 mL) was added dropwise at 0° C., over a period of 60 mins under nitrogen. The resulting solution was stirred at room temperature for 3 h. The reaction mixture was evaporated to dryness to afford the crude product (1.791 g) as a dark orange solid. The solid was redissolved in DCM and washed with NaHCO3. The organic layer was evaporated to dryness to afford methyl 4-(4-methylpiperazine-1-carbonyl)benzoate (0.890 g, 61.1%) as an orange gum, which solidified on standing. Used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737149B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-fb35064d694440779fad2aeb07bf3334
출처 메모uspto-grants-2010_06