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HRID 1779685作成日:2026年10月27日

Diethyl Carbonate → HCID 15591328、化合物

https://huagongshe.com/reaction/1779685

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl CarbonateHCID 7766—
反応物GlycidolHCID 11164—
反応物4-AminobenzonitrileHCID 13396—
反応物2-Methylpropan-2-olateHCID 4574913—
反応物p-(N-2,3-dihydroxypropylamino)benzonitrileHCID 10171309—
反応物3-(4-Cyanophenyl)-5-[4-(1,2-diethoxycarbonylethyl)piperazinomethyl)oxazolidin-2-oneHCID 70053592—
生成物HCID 15591328HCID 15591328—

反応手順

1.3 g of 3-(4-cyanophenyl)-5-[4-(1,2-diethoxycarbonylethyl)piperazinomethyl)oxazolidin-2-one [obtainable by reaction of 4-cyanoaniline with 2,3-epoxypropan-1-ol to give N-[4-cyanophenyl]-2,3-dihydroxypropylamine, reaction with diethyl carbonate in the presence of K tert-butoxide to give 3-(4-cyano-phenyl)-5-hydroxymethyloxazolidin-2-one, subsequent esterification with methanesulfonyl chloride and reaction with "B"] and 1.1 g of hydroxylamine hydrochloride are boiled for 2 hours in 125 ml of ethanol in the presence of 2.24 g of sodium ethoxide. The reaction mixture is then filtered and concentrated in vacuo. The residue is dissolved in water, the solution is adjusted to pH 3 using 2N hydrochloric acid and the resulting precipitate is filtered off with suction. After recrystallizing from water/glacial acetic acid, 3-[4-amino(hydroxyimino)methylphenyl]-5-[4-(1,2-diethoxycarbonylethyl)piperazinomethyl]oxazolidin-2-one, m.p. 186°, is obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05627197
出典データセットuspto-grants-1997_05
ORD IDord-76c6d531face45d185a05c464261ac34
出典メモuspto-grants-1997_05