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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 262157생성일: 2026년 10월 24일

Methyl iodide → 4-[[2-[(n-butylmethylamino)methyl]-1H-indol-3-yl]methyl]-2,4-dihydro-5-methyl-2-phenyl-3H-pyrazol-3-one

https://huagongshe.com/ko/reaction/262157

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물1H-Pyrazol-5-ol, 3-methyl-1-phenyl-HCID 70335—
반응물PyrazoloneHCID 11513733—
반응물2-n-Butyl-1,2,3,4-tetrahydropyrrolo[3,4-b]indoleHCID 21320255—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물4-[[2-[(n-butylmethylamino)methyl]-1H-indol-3-yl]methyl]-2,4-dihydro-5-methyl-2-phenyl-3H-pyrazol-3-oneHCID 70606689—

반응 단계

A solution of 2-n-Butyl-1,2,3,4-tetrahydropyrrolo[3,4-b]indole, 8.6 g., and methyl iodide, 2.6 ml. in dimethylformamide is stirred fifteen minutes, and then added all at once to a solution of the anion of the pyrazolone, prepared from 6.96 g. of 2-phenyl-5-methyl-3H-pyrazol-3-one and 2.0 g. fifty percent sodium hydride in dimethylformamide at 10°-20° C. The mixture is heated on a steam bath for one hour, then stirred at room temperature for sixteen hours. The reaction mixture is next poured into water, precipitating the product, 8.6 g., m.p. about 180°-200° with decomposition. Recrystallization from methanol gives 6.3 g., m.p. 195°-200° with decomposition.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04153711
출처 데이터셋uspto-grants-1979_05
ORD IDord-5242bf3ae1fa4368aaa68443bfd0a4f7
출처 메모uspto-grants-1979_05