돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 922381생성일: 2026년 10월 26일

Hydrochloric Acid → 6-(4-Propionylpiperazin-1-yl)picolinaldehyde

https://huagongshe.com/reaction/922381

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium CarbonateHCID 11430—
반응물6-Bromopyridine-2-carbaldehydeHCID 2757009—
반응물1-(Piperazin-1-yl)propan-1-oneHCID 3844375—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물6-(4-Propionylpiperazin-1-yl)picolinaldehydeHCID 8671934731%

반응 조건

온도120 °C

반응 단계

To a high-pressure tube was added 6-bromopicolinaldehyde (1, 2.00 g, 10.7 mmol), 1-(piperazin-1-yl)propan-1-one (18, 3.82 g, 26.9 mmol), potassium carbonate (6.69 g, 48.4 mmol) and anhydrous DMF (12 mL). The tube was sealed and the reaction mixture was heated at 120° C. for 17 h. The reaction suspension was poured into water (100 mL) and the mixture was brought to pH 7 using 2 N aq. HCl (20 mL). The solution was extracted with CH2Cl2 (3×100 mL), washed with brine (300 mL), dried over Na2SO4, filtered and concentrated to a brown oil. The product was purified by silica gel chromatography eluting with 0-5% CH3OH in CH2Cl2 to afford the title compound (0.815 g, 31%) as an orange solid: 1H NMR (500 MHz, CDCl3) δ 9.89 (s, 1H), 7.68 (t, J=8.0 Hz, 1H), 7.33 (d, J=8.0 Hz, 1H), 6.84 (d, J=8.0 Hz, 1H), 3.84-3.73 (m, 2H), 3.68-3.59 (m, 2H), 2.40 (q, J=7.5 Hz, 2H), 1.19 (t, J=7.5 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09278940B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-b6ecaa31adf24f61b19f43ae085f1262
출처 메모uspto-grants-2016_03