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6-Chloro-3-methyl-1-propyl-2,4(1H,3H)-pyrimidinedione → 6-Mercapto-3-methyl-1-propyl-pyrimidine-2,4(1H,3H)-dione
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 6-Chloro-3-methyl-1-propyl-2,4(1H,3H)-pyrimidinedione | HCID 816933 | — |
| 反応物 | Sodium hydrosulfide hydrate | HCID 16211346 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 6-Mercapto-3-methyl-1-propyl-pyrimidine-2,4(1H,3H)-dione | HCID 86622710 | — |
反応手順
A mixture of 6-chloro-3-methyl-1-propyl-pyrimidine-2,4(1H,3H)-dione (3.76 g), sodium hydrosulphide hydrate (6 g) and ethanol (100 ml) was stirred at room temperature for 48 hours then concentrated in vacuo. The residue was dissolved in water (500 ml) and washed with ethyl acetate (2×100 ml). The aqueous phase was acidified with dilute hydrochloric acid, then extracted with ethyl acetate (3×100 ml). The combined organic phase was dried (MgSO4) and evaporated to leave a pale yellow solid which was used directly in the next step.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07384950B2 |
| 出典データセット | uspto-grants-2008_06 |
| ORD ID | ord-aa2686d9fed644a8b4ea57c0b60b8015 |
| 出典メモ | uspto-grants-2008_06 |