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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43238생성일: 2026년 10월 25일

Pyridine → (7-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-2-oxo-3,4-dihydroquinolin-1(2H)-yl)methyl butyrate

https://huagongshe.com/reaction/43238

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Butyryl chlorideHCID 8855—
반응물N-Hydroxymethyl aripiprazoleHCID 58096483—
용매DichloromethaneHCID 6344—
생성물(7-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-2-oxo-3,4-dihydroquinolin-1(2H)-yl)methyl butyrateHCID 4985492495%

반응 단계

To a stirred suspension of Compound 2A (3 g, 6.27 mmol) in dichloromethane (30 mL) was added pyridine (2.54 mL, 31.35 mmol) followed by butyryl chloride (0.98 mL, 9.41 mmol) over 1-2 mins. The resultant solution was stirred at room temperature for 1 h 30 mins. The reaction was quenched with methanol (2 mL) and the mixture diluted with 1:1 NaHCO3 (aq)/brine (50 mL) and the layers separated. The aqueous layer was extracted with dichloromethane (10 mL) and the combined organics dried over MgSO4. After filtration, the volatiles were removed and the residue azeotroped with toluene (3×10 mL). The crude material was purified by silica chromatography eluting 8% Methanol/(1:1 ethyl acetate/dichloromethane) to provide the desired product, Compound 2B (3.26 g, 5.94 mmol, 95% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536328B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-bd92cf07e5824e099a26c573bbdce9f2
출처 메모uspto-grants-2013_09