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HRID 1489643作成日:2026年10月27日

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

https://huagongshe.com/reaction/1489643

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物3-[N-methyl-N-(2-{3,4-dimethoxy-phenyl}-ethyl)amino]-propanolHCID 15283521—
反応物5-(3,4-Dimethoxyphenyl)-pyrazolin-3-oneHCID 22046088—
反応物N-ethoxycarbonyliminocarbamateHCID 86599450—
溶媒TolueneHCID 1140—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物3-{3-[N-(2-(3,4-Dimethoxyphenyl)-ethyl)-N-methylamino]-propyloxy}-5-(3,4-dimethoxyphenyl)-pyrazoleHCID 1528352050.6%

反応条件

温度20 °C

反応手順

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 1E). 1.14 g of the title compound were obtained as an oily base. This base was converted as described in Example 1E), to the hydrochloride having a melting point of from 189° to 192° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05679699
出典データセットuspto-grants-1997_10
ORD IDord-9af12d34ba5b46c7af647e45e58b4ffb
出典メモuspto-grants-1997_10