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Diisopropylethylamine → 1-Benzyl 4-methyl 4-allylpiperidine-1,4-dicarboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | Benzyl succinimido carbonate | HCID 83172 | — |
| 反応物 | Methyl 4-allylpiperidine-4-carboxylate | HCID 66972977 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 1-Benzyl 4-methyl 4-allylpiperidine-1,4-dicarboxylate | HCID 58893186 | — |
反応手順
A mixture of methyl 4-allylpiperidine-4-carboxylate from Step A (5.30 g, 24.2 mmol), N-(benzyloxycarbonyloxy)succinimide (7.25 g, 29.1 mmol), and N,N-diisopropylethylamine (12.7 mL, 72.7 mmol) in CH3CN (61 mL) was stirred for 16 h. The solvent was removed in vacuo and the residue was partitioned between EtOAc (100 mL) and saturated NaHCO3 (100 mL). The organic layer was separated and the aqueous layer was further extracted with EtOAc (2×100 mL). The combined organic extracts were concentrated in vacuo to give a residue that was purified by silica gel chromatography, eluting with a gradient of hexane:EtOAc—100:0 to 40:60, to give the title compound. MS: m/z=318 (M+1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07893079B2 |
| 出典データセット | uspto-grants-2011_02 |
| ORD ID | ord-84147da71ee540f2a9dd29af4f9ce166 |
| 出典メモ | uspto-grants-2011_02 |