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(2-Thienylmethyl)amine → 2-(Pyrrolodin-2-one-1-ylmethyl)thiophene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | (2-Thienylmethyl)amine | HCID 34005 | — |
| 反応物 | Ethyl 4-bromobutyrate | HCID 76300 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | 2-(Pyrrolodin-2-one-1-ylmethyl)thiophene | HCID 67588803 | 47.6% |
反応手順
A mixture of ethyl 4-bromobutyrate (5.85 g, 30.0 mmol), 2-thiophenemethylamine (13.6 g, 120 mmol), and N,N-diisopropylethylamine (3.88 g, 30.0 mmol) in benzene (100 mL) was stirred under N2 at reflux for 2 hours. The reaction mixture was cooled to ambient temperature and filtered. The residue was concentrated in vacuo, dissolved in ether, and washed twice with 2N aqueous HCl, and once with brine, then dried over MgSO4, filtered, and concentrated in vacuo to give 2-(pyrrolodin-2-one-1-ylmethyl)thiophene (2.59 g) as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05616596 |
| 出典データセット | uspto-grants-1997_04 |
| ORD ID | ord-9c48b2d98f97457b9551f2e75bdadaf4 |
| 出典メモ | uspto-grants-1997_04 |