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HRID 50107作成日:2026年10月25日

Toluene → Methyl 4-(4-fluorophenyl)-6-(1-methylethyl)-2-(methyl(methylsulfonyl)amino)-5-pyrimidinecarboxylate

https://huagongshe.com/reaction/50107

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物N-cyano-N-methylmethanesulphonamideHCID 10219456—
反応物HCID 178500902HCID 178500902—
触媒Titanium TetrachlorideHCID 24193—
溶媒WaterHCID 962—
生成物Methyl 4-(4-fluorophenyl)-6-(1-methylethyl)-2-(methyl(methylsulfonyl)amino)-5-pyrimidinecarboxylateHCID 992982180.3%

反応条件

温度110 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06710178B2
出典データセットuspto-grants-2004_03
ORD IDord-0efebf0306204be49d7b2753b8d39b9e
出典メモuspto-grants-2004_03