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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42483생성일: 2026년 10월 23일

Cyanoacetamide → 4-Methyl-2-oxo-6-(phenylmethyl)-1,2-dihydro-3-pyridinecarbonitrile

https://huagongshe.com/ko/reaction/42483

반응식

참여 물질

역할이름HCID투입량
반응물CyanoacetamideHCID 7898—
반응물PiperidineHCID 8082—
반응물2,4-Pentanedione, 1-phenyl-HCID 18723—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물6-Methyl-2-oxo-4-(phenylmethyl)-1,2-dihydro-3-pyridinecarbonitrileHCID 67466801—
생성물4-Methyl-2-oxo-6-(phenylmethyl)-1,2-dihydro-3-pyridinecarbonitrileHCID 67467042103.4%

반응 조건

온도75 °C

반응 단계

1-Phenyl-2,4-pentanedione (18.32 g, 104 mmol) and cyanoacetamide (8.74 g, 104 mmol) were dissolved in EtOH (104 mL) and heated until homogenous (ca. 75° C.). Piperidine (8.86 g, 104 mmol) was added and the reaction mixture heated at reflux for 15-30 min. followed by cooling to room temperature, during which time precipitation occurred. The heterogenous contents were filtered to give a solid which was suspended in 200 mL water and stirred vigorously for 20 min. The heterogenous mixture was filtered to afford 6-methyl-2-oxo-4-(phenylmethyl)-1,2-dihydro-3-pyridinecarbonitrile and 4-methyl-2-oxo-6-(phenylmethyl)-1,2-dihydro-3-pyridinecarbonitrile (12.06 g, 52%). LCMS MH+=225.1

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536179B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-4a5291a1843c4cf5bf4c5ef412c25408
출처 메모uspto-grants-2013_09