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Diisopropylethylamine → Methyl (2S)-3-(4-biphenylyl)-2-[(2-isopropoxy-3,4-dioxocyclobut-1-enyl)amino]propanoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 3,4-Diisopropoxy-3-cyclobutene-1,2-dione | HCID 182314 | — |
| 反応物 | methyl (2S)-2-amino-3-(4-phenylphenyl)propanoate hydrochloride | HCID 45357110 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | Methyl (2S)-3-(4-biphenylyl)-2-[(2-isopropoxy-3,4-dioxocyclobut-1-enyl)amino]propanoate | HCID 86583676 | 64.1% |
反応手順
A mixture of methyl (2S)-2-amino-3-(4-biphenylyl)-propanoate hydrochloride (415 mg, 1142 mmol),3,4-diisopropoxy-3-cyclobutene-1,2-dione (281 mg, 1.42 mmol), DIPEA (247 μl, 1.42 mmol) and MeOH (10 ml) was stirred at room temperature overnight. The solvent was removed in vacuo and the residue purified by column chromatography (SiO2; DCM/MeOH, 98:2) to give the title compound (358 mg). δH (DMSO-d6, 390K) 8.50 (1H, d, J 8.0 Hz), 7.63-7.56 (4H, m), 7.47-7.42 (2H, m), 7.36-7.32 (3H, m), 5.24-5.18 (1H, m), 4.80-4.75 (1H, m), 3.74 (3H, s), 3.31 (1H, dd, J 14.2, 5.2 Hz), 3.13 (1H, dd, J, 14.2, 9.4 Hz), 1.38 (3H, d, J 6.0 Hz), 1.37 (3H, d, J 6.1 Hz); m/z (ES+, 70 V) 394 (MH+).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06455539B2 |
| 出典データセット | uspto-grants-2002_09 |
| ORD ID | ord-1cf98b4fc9a14b00a78dc177bfce27af |
| 出典メモ | uspto-grants-2002_09 |