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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4942생성일: 2026년 10월 23일

1-Methylpyrrolidine → 6-Ethyl-3-(4-hydroxymethyl-1-piperidinyl)pyridazine

https://huagongshe.com/ko/reaction/4942

반응식

참여 물질

역할이름HCID투입량
반응물1-MethylpyrrolidineHCID 8454—
반응물Ethyl 4-piperidinecarboxylateHCID 70770—
반응물DiisopropylethylamineHCID 81531—
반응물3-Bromo-6-ethylpyridazineHCID 19797309—
용매WaterHCID 962—
생성물6-Ethyl-3-(4-hydroxymethyl-1-piperidinyl)pyridazineHCID 19797306—

반응 조건

온도140 °C

반응 단계

1.67 g (0.011 mol) of 3-bromo-6-ethylpyridazine was added to 1.5 mL (10 mmol) ethyl isonipecotate and 3.5 mL (20 mmol) diisopropylethylamine and 5 mL N methylpyrrolidine (NMP). This mixture was heated to 140° C. for 4 hours. Upon cooling 100 mL of water was added to the mixture and the contents were extracted with methylene chloride then washed twice with water and once with brine and the solvent evaporated in vacuo. The resulting oil was eluted through a short silica gel plug with 80% ethyl acetate and 20% hexanes and dried in vacuo. This intermediate was taken up in 25 mL THF and was exposed to 3-fold excess lithium aluminum hydride with stirring under nitrogen for 1 hour. The reaction was chilled on ice and quenched by dropwise addition of water. The slurry was dried, treated with charcoal and filtered yielding 6-ethyl-3-(4-hydroxymethyl-1-piperidinyl)pyridazine (Formula IV: R1 =C2H5 ; Y=CH2 ).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05242924
출처 데이터셋uspto-grants-1993_09
ORD IDord-e7615e51d1964e48ab83367a353ca96f
출처 메모uspto-grants-1993_09