関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Toluene | HCID 1140 | — |
| 反応物 | N-cyano-N-methylmethanesulphonamide | HCID 10219456 | — |
| 反応物 | HCID 178500902 | HCID 178500902 | — |
| 触媒 | Titanium Tetrachloride | HCID 24193 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | Methyl 4-(4-fluorophenyl)-6-(1-methylethyl)-2-(methyl(methylsulfonyl)amino)-5-pyrimidinecarboxylate | HCID 9929821 | 80.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US06579984B1 |
|---|
| 出典データセット | uspto-grants-2003_06 |
|---|
| ORD ID | ord-a88c99e6b92846ce873a7ea338fac563 |
|---|
| 出典メモ | uspto-grants-2003_06 |
|---|