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1-(1-Piperidinylcarbonyl)piperazine → 2-[4-(Piperidine-1-carbonyl)piperazin-1-yl]-5,6,7,8-tetrahydro-3H-quinazolin-4-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-(1-Piperidinylcarbonyl)piperazine | HCID 1095015 | — |
| 反応物 | 2-(Methylthio)-5,6,7,8-tetrahydroquinazolin-4(3H)-one | HCID 135435256 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 溶媒 | Isoamyl Alcohol | HCID 31260 | — |
| 生成物 | 2-[4-(Piperidine-1-carbonyl)piperazin-1-yl]-5,6,7,8-tetrahydro-3H-quinazolin-4-one | HCID 136268342 | — |
反応手順
2-Methylsulfanyl-5,6,7,8-tetrahydro-3H-quinazolin-4-one (100 mg; 0.51 mmol) and piperazin-1-ylpiperidin-1-ylmethanone (100.5 mg; 0.51 mmol) are reacted in isoamyl alcohol (1 ml) in accordance with the procedure for Example 1. After a reaction time of 4 h, piperazin-1-ylpiperidin-1-ylmethanone (50.3 mg; 0.26 mmol) and isoamyl alcohol (0.5 ml) are again added, and the mixture is again irradiated in the microwave for 4 h. The crystals obtained after conventional work-up are dissolved in acetonitrile and water and freeze-dried; yield: 17 mg (9%), crystals;
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09339503B2 |
| 出典データセット | uspto-grants-2016_05 |
| ORD ID | ord-b6969258110b4179bb87e069ddf3fd81 |
| 出典メモ | uspto-grants-2016_05 |