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N-Hydroxyphthalimide → (2-Tritylamino-4-thiazolyl)methoxyphthalimide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | N-Hydroxyphthalimide | HCID 10665 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 4-Chloromethyl-2-tritylaminothiazole | HCID 13745172 | — |
| 触媒 | Dicyclohexano-18-crown-6 | HCID 85955 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | (2-Tritylamino-4-thiazolyl)methoxyphthalimide | HCID 21285061 | 96.1% |
反応手順
8.15 g of N-hydroxyphthalimide was dissolved in 300 ml of N,N-dimethylformamide, 6.91 g of potassium carbonate and 200 mg of dicyclohexyl-18-crown-6 were added, and stirred at room temperature for 2 hours. Thereafter, 9.82 g of 4-chloromethyl-2-tritylaminothiazol was added thereto, and stirred and reacted at room temperature for 8 hours. The reaction mixture was concentrated under reduced pressure, and, after adding 500 ml of ethyl acetate, washed with 300 ml of water 4 times. The ethyl acetate layer was dried on anhydrous magnesium sulfate, and concentrated to dryness to obtain 12.5 g of (2-tritylaminothiazol-4-yl)methoxyphthalimide.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04785090 |
| 出典データセット | uspto-grants-1988_11 |
| ORD ID | ord-45a65fe7a25b40b08ba6844b4201d3f1 |
| 出典メモ | uspto-grants-1988_11 |