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Triethylamine → 4-(3-Methyl-2-nitrophenyl)-piperazine-1-carboxylic acid tert-butyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| 反応物 | 3-Methyl-2-nitrophenyl trifluoromethanesulphonate | HCID 15869552 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 4-(3-Methyl-2-nitrophenyl)-piperazine-1-carboxylic acid tert-butyl ester | HCID 60108775 | 37.5% |
反応手順
Trifluoromethanesulfonic acid 3-methyl-2-nitrophenyl ester (26.7 g, 93.6 mmol), 1-tert-butoxycarbonyl piperazine (17 g, 91.3 mmol) and triethylamine (14 mL, 100 mmol) in 250 mL of acetonitrile was heated under reflux for 25 h. The mixture was concentrated in vacuo, diluted with water and extracted with ether. The ether was washed with aqueous ammonium hydroxide and brine, dried, and evaporated. Purification by silica gel chromatography (10% ethyl acetate-hexane) afforded 11 g of 4-(3-methyl-2-nitrophenyl)-piperazine-1-carboxylic acid tert-butyl ester as a golden solid, m.p. 101-102° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06787535B2 |
| 出典データセット | uspto-grants-2004_09 |
| ORD ID | ord-fef11ca5a52242f8bab6da1a7db8c076 |
| 出典メモ | uspto-grants-2004_09 |