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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1078342생성일: 2026년 10월 26일

Triphenylphosphine → 3-{3-[N-(2-(3,4-Dimethoxyphenyl)-ethyl)-N-methylamino]-propyloxy}-5-(3,4-dimethoxyphenyl)-pyrazole

https://huagongshe.com/reaction/1078342

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참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물3-[N-methyl-N-(2-{3,4-dimethoxy-phenyl}-ethyl)amino]-propanolHCID 15283521—
반응물5-(3,4-Dimethoxyphenyl)-pyrazolin-3-oneHCID 22046088—
반응물N-ethoxycarbonyliminocarbamateHCID 86599450—
용매TolueneHCID 1140—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물3-{3-[N-(2-(3,4-Dimethoxyphenyl)-ethyl)-N-methylamino]-propyloxy}-5-(3,4-dimethoxyphenyl)-pyrazoleHCID 1528352050.6%

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온도20 °C

반응 단계

1.31 g of triphenylphosphine were dissolved in 15 ml of tetrahydrofuran. 1.6 ml of a solution of 0.8 ml of ethyl azodicarboxylate in 0.8 ml of toluene were added dropwise to the solution at a temperature of 5° C. After 5 minutes a solution of 1.1 g of 5-(3,4-dimethoxyphenyl)-pyrazolin-3-one in 10 ml of dimethylformamide was added dropwise. After 20 minutes a solution of 1.26 g of 3-[N-(2-(3,4-dimethoxyphenyl)-ethyl)-N-methylamino]-propanol in 10 ml of tetrahydrofuran was added dropwise. The reaction mixture was subsequently stirred at 20° C. for 48 hours. The reaction mixture was then evaporated to dryness. The resulting crude product was purified by flash chromatography in accordance with the method described in Example 1 E). 1.14 g of the title compound were obtained as an oily base. This base was converted as described in Example 1 E), to the hydrochloride having a melting point of from 189° to 192° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05547967
출처 데이터셋uspto-grants-1996_08
ORD IDord-576124c74dab4f82971ae826d2f08197
출처 메모uspto-grants-1996_08