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Diethyl (ethoxymethylene)malonate → Diethyl N-[2-(2-pyridinyl)-4-pyrimidinyl]aminomethylenemalonate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| 反応物 | 2-(Pyridin-2-yl)pyrimidin-4-amine | HCID 12403616 | — |
| 反応物 | diethyl N-[2-(2-pyridinyl)-4-pyrimidinyl]aminomethylenemalonate methanesulfonate | HCID 12764726 | — |
| 生成物 | Diethyl N-[2-(2-pyridinyl)-4-pyrimidinyl]aminomethylenemalonate | HCID 12764725 | — |
反応手順
A mixture containing 8.7 g. of 4-amino-2-(2-pyridinyl)pyrimidine and 14.2 g. of diethyl ethoxymethylenemalonate was heated in an oil bath at 130°-140° C. for one hour and then cooled to room temperature. To the cooled reaction mixture was added with stirring 300 ml. of ether and the mixture was filtered. To the filtrate was added 4.8 g. of methanesulfonic acid dissolved in 25 ml. of ethanol whereupon there separated an oily material which became a crystalline solid on standing. The solid was collected and recrystallized from ether-ethanol to yield 10.4 g. of diethyl N-[2-(2-pyridinyl)-4-pyrimidinyl]aminomethylenemalonate methanesulfonate, m.p. 162°-164° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04032523 |
| 出典データセット | uspto-grants-1977_06 |
| ORD ID | ord-ad6d4ba8d1404c4284d2c37bdce2a126 |
| 出典メモ | uspto-grants-1977_06 |