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3,5-Dimethylbenzenethiol → Ethyl 4-[(3,5-dimethylphenyl)-thio]-1,6-dihydro-2-methyl-6-oxo-3-pyridinecarboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3,5-Dimethylbenzenethiol | HCID 117548 | — |
| 反応物 | Ethyl 4-chloro-2-methyl-6-oxo-1,6-dihydro-3-pyridinecarboxylate | HCID 21935322 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | Ethyl 4-[(3,5-dimethylphenyl)-thio]-1,6-dihydro-2-methyl-6-oxo-3-pyridinecarboxylate | HCID 21935307 | — |
反応手順
A mixture of the intermediate 13 (1.2 g; 5.6 mmol) in ethanol (15 ml), triethylamine (1.5 ml) and 3,5-dimethylthiophenol (1.45 ml; 11 mmol) was heated under reflux for 16 hours. After evaporation under reduced pressure, diethylether (50 ml) was added and the precipitate was filtered off. The intermediate 14 was obtained (1.42 g; 80%) as a colorless solid m.p.=233–235° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07115608B2 |
| 出典データセット | uspto-grants-2006_10 |
| ORD ID | ord-91805880c0424cffb923e923189a3dfb |
| 出典メモ | uspto-grants-2006_10 |