関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | N-3-Bromopropylphthalimide | HCID 21611 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Diethyl 3,4-pyrroledicarboxylate | HCID 688199 | — |
| 生成物 | 1-N-Propylphthalimido-1H-pyrrole-3,4-dicarboxylate diethyl ester | HCID 69734830 | 92% |
反応手順
A solution of diethyl pyrrole-3,4-dicarboxylate (39 g, 0.185 mol) in THF (1600 mL) was treated with NaH (60%, 7.6 g, 0.19 mol). The reaction mixture was heated to reflux for 1 hour. The reaction was then cooled to 30° C. and N-(3-bromopropyl)phthalimide (52 g, 0.19 mol) was added. The reaction mixture was heated to reflux for 1 hour, cooled, filtered, and concentrated in vacuo. The resultant gum was partitioned between ETOAC/H2O and extracted with EtOAC (2×300 mL). The organic layer was dried (MgSO4), filtered and concentrated in vacuo. The resultant solid was recrystallized from EtOAC to give the title compound 68 g (92%) (mp 100-101° C.). 1H NMR (DMSO) δ1.24 (t, 3H, CH), 2.06 (m, 2H, CH3), 3.57 (t, 2H, CH2), 4.14 (m, 4H, CH2), 7.49 (s, 2H, ArH), 7.86 (m, 4H, ArH).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06559303B1 |
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| 出典データセット | uspto-grants-2003_05 |
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| ORD ID | ord-7a5c14fb13504cb7981f31b02585e278 |
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| 出典メモ | uspto-grants-2003_05 |
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