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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1431433생성일: 2026년 10월 27일

Formaldehyde → 1-(4-Chloro-5,7-difluoro-3-methylquinolin-2-yl)-4-methylpiperazin-2-one

https://huagongshe.com/reaction/1431433

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물1-(4-Chloro-5,7-difluoro-3-methylquinolin-2-yl)piperazin-2-oneHCID 59631389—
용매MethanolHCID 887—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매1,1-DichloroethaneHCID 6365—
생성물1-(4-Chloro-5,7-difluoro-3-methylquinolin-2-yl)-4-methylpiperazin-2-oneHCID 59631317—

반응 단계

The 1-(4-chloro-5,7-difluoro-3-methylquinolin-2-yl)piperazin-2-one (52.0 mg, 0.167 mmol) and paraformaldehyde (5.01 mg, 0.167 mmol) were dissolved in 1.5 mL of a 2:1 dichloroethane:MeOH solution. The sodium triacetoxyborohydride (106 mg, 0.500 mmol) was added and the reaction mixture was stirred for 6.5 h. The reaction by LCMS had only progressed ˜30%. Some sodium cyanoborohydride (50 mg, 0.796 mmol) was added turning the mixture into a solution again and stirred overnight. The reaction was then diluted with DCM and water. The layers were separated and the organic layer was washed with brine (1×10 mL) and dried over magnesium sulfate to give crude 1-(4-chloro-5,7-difluoro-3-methylquinolin-2-yl)-4-methylpiperazin-2-one. Mass Spectrum (ESI) m/e=312.1 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08940724B2
출처 데이터셋uspto-grants-2015_01
ORD IDord-59238b8b1a8a4eb196186884b4b7af87
출처 메모uspto-grants-2015_01