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HRID 417226생성일: 2026년 10월 27일

Piperidine → Z-6-chloro-3-(3-chloro-2-fluoro-benzylidene)-4-fluoro-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/417226

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참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물3-Chloro-2-fluorobenzaldehydeHCID 736335—
반응물6-Chloro-4-fluoroindolin-2-oneHCID 66634278—
용매MethanolHCID 887—
생성물Z-6-chloro-3-(3-chloro-2-fluoro-benzylidene)-4-fluoro-1,3-dihydro-indol-2-oneHCID 8665393574.8%

반응 조건

온도50 °C

반응 단계

To the mixture of 6-chloro-4-fluoroindolin-2-one (Natrochem, 85% purity) (1.1 g, 5.0 mmol) and 3-chloro-2-fluorobenzaldehyde (2.4 g, 15 mmol) (Oakwood) in methanol (50 mL) was added piperidine (1.7 g, 20 mmol) (Aldrich) dropwise. The mixture was then heated at 50° C. for 3 h. After cooled to 4° C., the mixture was filtered and resulting precipitate was collected, washed with cold methanol, dried to give the first batch of desired product (1.22 g). The filtrate was concentrated, and the residue was partitioned between ethyl acetate and water. The organic layer was separated, washed with water, brine, dried over MgSO4, and concentrated. The residue was purified by chromatography (20-35% EtOAc in hexanes) to give the second batch of desired product (0.32 g). The two batches were combined to give E/Z-6-chloro-3-(3-chloro-2-fluoro-benzylidene)-4-fluoro-1,3-dihydro-indol-2-one as a yellow solid (Yield 1.54 g, 94%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08088815B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-1a524774307d45fa97ae122e6351b988
출처 메모uspto-grants-2012_01