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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 982613생성일: 2026년 10월 25일

Acrylonitrile → HCID 22562162, 화합물

https://huagongshe.com/reaction/982613

반응식

참여 물질

역할이름HCID투입량
반응물AcrylonitrileHCID 7855—
반응물TriethylamineHCID 8471—
반응물2,2,2-trifluoro-N-(piperidin-4-yl)acetamideHCID 10774253—
용매TetrahydrofuranHCID 8028—
생성물HCID 22562162HCID 2256216230%

반응 단계

A mixture of 3 g (15.3 mmol) of 4-trifluoroacetamidopiperidine, 3 g (4.25 mL, 30.6 mmol) of triethylamine, 3 mL (45.9 mmol) of acrylonitrile in 10 mL of THF was stirred at room temperature for 17 hr. The solvent and volatile were evaporated under reduced pressure. The residue was dissolved in 20 mL of methanol and 4 mL of 30% NH4OH and the solution was refluxed for 5 hr. The solvent was evaporated under reduced pressure and the residue was purified by column chromatography on silica gel eluting first with 500 mL of dichloromethane, then 500 mL of 0.5% methanol/dichloromethane, followed by 1000 mL of 9:1:0.1 dichloromethane/methanol/ammonium hydroxide to give 0.7 g (30% yield) of the N-(2-cyanoethyl)-4-aminopiperidine. Step 4: Preparation of 6-(2-chlorophenyl)-2-(N-2-cyanoethylpiperidyl-4-amino)-pyrido[2,3-d]-pyrimidin-7-ol

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06861423B2
출처 데이터셋uspto-grants-2005_03
ORD IDord-8c3f64fbee9441ae8730b14989629cfd
출처 메모uspto-grants-2005_03