Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1369963생성일: 2026년 10월 25일
Sodium hydride → Methyl 4-(4-fluorophenyl)-6-(1-methylethyl)-2-(methyl(methylsulfonyl)amino)-5-pyrimidinecarboxylate
https://huagongshe.com/reaction/1369963
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Dimethylacetamide | HCID 31374 | — |
| 반응물 | N-cyano-N-methylmethanesulphonamide | HCID 10219456 | — |
| 반응물 | HCID 178500902 | HCID 178500902 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | Methyl 4-(4-fluorophenyl)-6-(1-methylethyl)-2-(methyl(methylsulfonyl)amino)-5-pyrimidinecarboxylate | HCID 9929821 | 29.1% |
반응 단계
2.66 g (10.0 mmol) of methyl 2-[1-amino-1-(4-fluorophenyl)methylene]-4-methyl-3-oxopentanoate were introduced into 12 g of N,N-dimethylacetamide together with 2.70 g (20.0 mmol) of N-cyano-N-methylmethanesulphonamide. 440 mg (11.0 mmol) of sodium hydride (60% in oil) were added to this solution at room temperature over the course of 2 h. An orange-red clear solution was obtained. After 6 h at room temperature, the reaction solution was poured onto 25 ml of water. The suspension was stirred in an ice bath for 30 minutes, and the precipitate was filtered off and washed with water (2×10 ml). After drying in a high vacuum, 1.11 g (29.1%) of methyl 4-(4-fluorophenyl)-6-isopropyl-2-(N-methanesulphonyl-N-methylamino)pyrimidine-5-carboxylate were obtained in the form of a pale beige solid. The product still contained traces of methyl 2-[1-amino-1-(4-fluorophenyl)methylene]-4-methyl-3-oxopentanoate.
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-ba404f0fb2204f88a6df4bb4afb1b514 |
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| 출처 메모 | uspto-grants-2003_06 |
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