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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2368362생성일: 2026년 10월 26일

Azetidine → Azetidin-1-yl(2-methyl-4-nitro-2H-pyrazol-3-yl)methanone

https://huagongshe.com/reaction/2368362

반응식

참여 물질

역할이름HCID투입량
반응물AzetidineHCID 10422—
반응물DiisopropylethylamineHCID 81531—
반응물Propylphosphonic anhydrideHCID 111923—
반응물1-Methyl-4-nitro-1H-pyrazole-5-carboxylic acidHCID 592623—
용매Ethyl AcetateHCID 8857—
생성물Azetidin-1-yl(2-methyl-4-nitro-2H-pyrazol-3-yl)methanoneHCID 7009694473.1%

반응 단계

To a suspension of 2-methyl-4-nitro-2H-pyrazole-3-carboxylic acid (300 mg, 1.75 mmol), azetidine (354 μl, 5.25 mmol) and diisopropylethylamine (920 μl, 5.26 mmol) in ethyl acetate (7.5 ml) was added 1-propanephosphonic acid cyclic anhydride (3.68 ml, 6.13 mmol; 50% in ethyl acetate) at 0° C. The ice bath was removed and stirring at r.t. was continued for 40 h. The reaction mixture was poured into ethyl acetate (100 ml) and extracted with sodium bicarbonate (saturated aqueous solution) water and brine. The aqueous layer was back-extracted with ethyl acetate, the combined organic phases were dried, evaporated, and the product was purified by silica gel chromatography using an amine phase and a heptane/ethyl acetate gradient to yield a white solid (269 mg, 73%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08703768B2
출처 데이터셋uspto-grants-2014_04
ORD IDord-1e51b48315954a17ba5b8285fb84a243
출처 메모uspto-grants-2014_04