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Tributylphosphine → 5-chloro-3-(3-chlorobenzyl)-N-[1-(4-cyanophenyl)ethyl]thiophene-2-carboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tributylphosphine | HCID 13831 | — |
| 反応物 | Diphenyl diselenide | HCID 15460 | — |
| 反応物 | 4'-Cyanoacetophenone | HCID 74044 | — |
| 反応物 | 5-Chloro-3-(3-chlorobenzyl)thiophene-2-carboxylic acid | HCID 45140204 | — |
| 反応物 | 4-(1-Azidoethyl)benzonitrile | HCID 57900982 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 5-chloro-3-(3-chlorobenzyl)-N-[1-(4-cyanophenyl)ethyl]thiophene-2-carboxamide | HCID 57900981 | — |
反応手順
To a suspension of 5-chloro-3-(3-chlorobenzyl)thiopbene-2-carboxylic acid from Example 1, Step 6 (230 mg, 0.801 mmol), 4-(1-azidoethyl)benzonitrile (146 mg, 0.848 mmol) [prepared according to Thompson et al. J. Org. Chem. 1993, 58, 5886, after reduction of commercially available 4-acetylbenzonitrile] and diphenyl diselenide (549 mg, 1.76 mmol) in acetonitrile at r.t. under N2 was added tributylphosphine (217 μL, 0.881 mmol, 1.1 eq) dropwise (suspension dissolved, slightly exothermic) and the mixture was stirred at r.t. for 6 h, quenched with saturated NaHCO3 and extracted with ether. The crude was purified by Combi Flash chromatography system (10-40% EtOAc/hexane) to give the desired product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08969394B2 |
| 出典データセット | uspto-grants-2015_03 |
| ORD ID | ord-27512fc6ee68476f8bc87d3b9152fbd4 |
| 出典メモ | uspto-grants-2015_03 |