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(4-Ethoxy-3-fluorophenyl)boronic acid → 1,1-Dimethylethyl 4-(4-ethoxy-3-fluorobenzoyl)-1-piperidinecarboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | (4-Ethoxy-3-fluorophenyl)boronic acid | HCID 2782821 | — |
| 反応物 | 4-Phenylsulfanylcarbonyl-piperidine-1-carboxylic acid tert-butyl ester | HCID 89375800 | — |
| 触媒 | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| 触媒 | Cuprous 2-thiophenecarboxylate | HCID 11194830 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1,1-Dimethylethyl 4-(4-ethoxy-3-fluorobenzoyl)-1-piperidinecarboxylate | HCID 71226782 | 82.6% |
反応手順
To a mixture of 4-ethoxy-3-fluorophenylboronic acid (0.86 g, 4.67 mmol), ligand TFP (0.144 g, 0.62 mmol), Pd2dba3 (0.29 g, 0.31 mmol), copper (I) thiophene-2-carboxylate (0.89 g, 4.7 mmol) was added a solution of 4-phenylsulfanylcarbonyl-piperidine-1-carboxylic acid tert-butyl ester (1.0 g, 3.11 mmol) in 10 mL of THF while purging with N2 at 50° C. After 18 hours the reaction mixture was diluted with ethyl acetate, filtered through celite then concentrated in vacuo. Purification by flash chromatography gave the title compound (0.95 g, 2.57 mmol). MS (ESI) m/z 352.0 (M+H+); HPLC (Novapak 150×3.9 mm C-18 column: mobile phase: 35-90% acetonitrile/water with 0.1% TFA, at 2 mL/min over 2 min.) t 1.42 min.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09181266B2 |
| 出典データセット | uspto-grants-2015_11 |
| ORD ID | ord-d0bd7f4aa1404a8b81ccc81c987bd368 |
| 出典メモ | uspto-grants-2015_11 |