Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1369964생성일: 2026년 10월 24일
Toluene → Methyl 4-(4-fluorophenyl)-6-(1-methylethyl)-2-(methyl(methylsulfonyl)amino)-5-pyrimidinecarboxylate
https://huagongshe.com/ko/reaction/1369964
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Toluene | HCID 1140 | — |
| 반응물 | N-cyano-N-methylmethanesulphonamide | HCID 10219456 | — |
| 반응물 | HCID 178500902 | HCID 178500902 | — |
| 촉매 | Titanium Tetrachloride | HCID 24193 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | Methyl 4-(4-fluorophenyl)-6-(1-methylethyl)-2-(methyl(methylsulfonyl)amino)-5-pyrimidinecarboxylate | HCID 9929821 | 80.3% |
반응 단계
10.0 g (37.7 mmol) of methyl 2-[1-amino-1-(4-fluorophenyl)methylene]-4-methyl-3-oxopentanoate were introduced into 50 ml of toluene together with 10.17 g (75.4 mmol) of N-cyano-N-methylmethanesulphonamide and the mixture was treated at room temperature with 3.61 g (18.9 mmol) of titanium tetrachloride. The reaction progressed exothermically. The red-orange-coloured suspension was heated to 110° C. and stirred for 4.5 h. It was then cooled to room temperature and treated with 30 ml of water. The organic phase was separated off and the aqueous phase was extracted with ethyl acetate (30 ml). The combined organic phases were washed with 30 ml of water and dried over magnesium sulphate. After filtering and concentrating the solution in a water-jet vacuum and drying in vacuo, 11.54 g of crude product were obtained in the form of a tacky oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06579984B1 |
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| 출처 데이터셋 | uspto-grants-2003_06 |
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| ORD ID | ord-a88c99e6b92846ce873a7ea338fac563 |
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| 출처 메모 | uspto-grants-2003_06 |
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