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N-bromobutanimide → 5-bromo-6-chloro-2-(methylthio)-N-(prop-2-ynyl)pyrimidine-4-amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | N-bromobutanimide | HCID 67184 | — |
| 反応物 | 6-chloro-2-(methylthio)-N-(prop-2-ynyl)pyrimidine-4-amine | HCID 90303691 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 5-bromo-6-chloro-2-(methylthio)-N-(prop-2-ynyl)pyrimidine-4-amine | HCID 90303713 | — |
反応手順
To a stirring solution of 1.16 g (5.45 mmol) of 6-chloro-2-(methylthio)-N-(prop-2-ynyl)pyrimidine-4-amine (intermediate 27) in 6 ml of DCM, 1.07 g (6.0 mmol) of N-bromosuccinimide were added, and stirring was continued for 4 hours at room temperature to give 5-bromo-6-chloro-2-(methylthio)-N-(prop-2-ynyl)pyrimidine-4-amine, which was used without further purification in the next step (see intermediate 31). The completion of the reaction is monitored by thin layer chromatography.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09447095B2 |
| 出典データセット | uspto-grants-2016_09 |
| ORD ID | ord-b8e265fff5ff4cec976cdc1e7c51ab0f |
| 出典メモ | uspto-grants-2016_09 |