関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Sodium methanethiolate | HCID 4378561 | — |
| 反応物 | 6-chloro-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinone | HCID 19690700 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 5-methyl-2-phenyl-3-propargyl-6-methylthio-4(3H)-pyrimidinone | HCID 19690712 | — |
反応手順
To a solution of 2.5 g (9.67 mmol) of 6-chloro-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinone in 100 mL of methanol, was added 0.8 g (11.4 mmol) sodium thiomethoxide and the reaction was stirred at room temperature for 4 days. The methanol was evaporated and the residue was dissolved in 100 mL of ethyl acetate, then washed three times with 50 mL of 1M sodium hydroxide followed by one time with 50 mL of brine. The organic layer was dried over MgSO4 and concentrated to yield 2.6 g crude product. Flash column chromatography on silica gel (100% methylene chloride) afforded 5-methyl-2-phenyl-3-propargyl-6-thiomethyl-4(3H)-pyrimidinone (Compound 26) as a white solid. 1H-NMR (CDCl3) δ2.1 (3H, s); 2.35 (1H, t); 2.5 (3H, s); 4.55 (2H, d); 7.5 (3H, m); 7.7 (2H, m).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05300477 |
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| 出典データセット | uspto-grants-1994_04 |
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| ORD ID | ord-377906cb16a849deaf5e8ad5fe6ba6e2 |
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| 出典メモ | uspto-grants-1994_04 |
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