Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1030생성일: 2026년 10월 25일
Hydrogen Sulfide → 3-p-Amidinophenyl-5-(p-methoxycarbonylmethylphenoxymethyl)oxazolidin-2-one
https://huagongshe.com/reaction/1030
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrogen Sulfide | HCID 402 | — |
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | 3-p-Cyanophenyl-5-(p-methoxycarbonyimethylphenoxymethyl)oxazolidin-2-one | HCID 15281528 | — |
| 용매 | Triethylamine | HCID 8471 | — |
| 생성물 | 3-p-Amidinophenyl-5-(p-methoxycarbonylmethylphenoxymethyl)oxazolidin-2-one | HCID 19356317 | — |
반응 단계
H2S gas is passed, at -10°, into a solution of 1.2 g of 3-p-cyanophenyl-5-(p-methoxycarbonyimethylphenoxymethyl)oxazolidin-2-one (obtainable in accordance with Example 1) in 50 ml of pyridine and 7 ml of triethylamine. The mixture is subsequently stirred at room temperature for 14 h and concentrated by evaporation; the residue is dissolved in 50 ml of acetone and treated with 9 ml of methyl iodide. After this mixture has been stirred for a further 6 h, it is filtered and the residue is washed with 5 ml of acetone and dissolved in 30 ml of methanol; 4.6 g of ammonium acetate are added to this solution, which is stirred at room temperature for 24 h. Following the customary working-up, 3-p-amidinophenyl-5-(p-methoxycarbonylmethylphenoxymethyl)oxazolidin-2-one (semihydriodide) is obtained, M.p. 151°-152°.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05723480 |
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| 출처 데이터셋 | uspto-grants-1998_03 |
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| ORD ID | ord-b93694f35b514da089ea14094910a4e3 |
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| 출처 메모 | uspto-grants-1998_03 |
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