関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1-Butanol | HCID 263 | — |
| 反応物 | 4-Chloro-6-(chloromethyl)pyrimidin-2-amine | HCID 20153488 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 生成物 | 2-Amino-4-n-butoxy-6-chloromethylpyrmidine | HCID 54521493 | — |
反応手順
3,56 Parts of 2-amino-4-chloro-6-chloromethylpyrimidine and 2.24 parts of potassium t-butoxide were dissolved in 60 parts of n-butanol at room temperature then the solution was heated at 50° C. for 2 hours, with stirring. After this time, the solution was cooled and evaporated in vacuo. The residue was partitioned between ethyl acetate and water and the organic phase was separated and washed three times with water then dried (MgSO4). Evaporation of the solvent gave the crude product which was purified by chromatography on silica (Merck Kieselgel 60) eluted with ether to give 2-amino-4-n-butoxy-6-chloromethylpyrmidine as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US04723006 |
|---|
| 出典データセット | uspto-grants-1988_02 |
|---|
| ORD ID | ord-c5c4f3d95a07449791cf3a5bbb4138ec |
|---|
| 出典メモ | uspto-grants-1988_02 |
|---|