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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Butyryl chloride | HCID 8855 | — |
| 반응물 | N-Hydroxymethyl aripiprazole | HCID 58096483 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (7-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-2-oxo-3,4-dihydroquinolin-1(2H)-yl)methyl butyrate | HCID 49854924 | 95% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08536328B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-bd92cf07e5824e099a26c573bbdce9f2 |
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| 출처 메모 | uspto-grants-2013_09 |
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