참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diethyl Carbonate | HCID 7766 | — |
| 반응물 | Glycidol | HCID 11164 | — |
| 반응물 | 4-Aminobenzonitrile | HCID 13396 | — |
| 반응물 | 2-Methylpropan-2-olate | HCID 4574913 | — |
| 반응물 | p-(N-2,3-dihydroxypropylamino)benzonitrile | HCID 10171309 | — |
| 반응물 | 3-(4-Cyanophenyl)-5-[4-(1,2-diethoxycarbonylethyl)piperazinomethyl)oxazolidin-2-one | HCID 70053592 | — |
| 생성물 | HCID 15591328 | HCID 15591328 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US05627197 |
|---|
| 출처 데이터셋 | uspto-grants-1997_05 |
|---|
| ORD ID | ord-76c6d531face45d185a05c464261ac34 |
|---|
| 출처 메모 | uspto-grants-1997_05 |
|---|