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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

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물DimethylacetamideHCID 31374—
반응물N-cyano-N-methylmethanesulphonamideHCID 10219456—
반응물HCID 178500902HCID 178500902—
용매WaterHCID 962—
생성물Methyl 4-(4-fluorophenyl)-6-(1-methylethyl)-2-(methyl(methylsulfonyl)amino)-5-pyrimidinecarboxylateHCID 992982129.1%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06579984B1
출처 데이터셋uspto-grants-2003_06
ORD IDord-ba404f0fb2204f88a6df4bb4afb1b514
출처 메모uspto-grants-2003_06