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Methanethiol → 2-Amino-4-fluoromethyl-6-methylthiopyrimidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methanethiol | HCID 878 | — |
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Sodium | HCID 5360545 | — |
| 反応物 | 4-Fluoro-6-(fluoromethyl)pyrimidin-2-amine | HCID 20153498 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 2-Amino-4-fluoromethyl-6-methylthiopyrimidine | HCID 20153491 | — |
反応手順
A mixture of 1.0 part of 2-amino-4-fluoro-6-fluoromethylpyrimidine, 3.0 parts of methanethiol and 50 parts of dry tetrahydrofuran was stirred at 5° C. whilst a solution of 0.16 parts of sodium in 20 parts of dry methanol was added dropwise. The temperature was kept below 10° C. with ice-bath cooling. When the addition was complete, stirring was continued for 1 hour. The resulting solution was evaporated and the residue was diluted with water and extracted three times with 50 parts of ether. The ethereal solutions were combined and dried (MgSO4). The solvent was evaporated and the crude product was purified by recrystallisation from carbon tetrachloride to give 2-amino-4-fluoromethyl-6-methylthiopyrimidine m.p. 95°-97° C.
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-2890b78e01af42029f6cf55bc787a012 |
| 出典メモ | uspto-grants-1988_02 |