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3-Fluoro-4-hydroxybenzeneacetic acid → N-Benzyl-2-(3-fluoro-4-hydroxyphenyl)-N-hexylacetamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 3-Fluoro-4-hydroxybenzeneacetic acid | HCID 68014 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | Benzenemethanamine, N-hexyl- | HCID 485395 | — |
| 反応物 | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | N-Benzyl-2-(3-fluoro-4-hydroxyphenyl)-N-hexylacetamide | HCID 68871257 | 77.2% |
反応手順
3-Fluoro-4-hydroxyphenylacetic acid (170 mg, 0.999 mmol) dissolved in DMF (3 ml) was cooled in an ice-bath N-Hexylbenzylamine (201 mg, 1.049 mmol) was added and then TBTU (337 mg, 1.049 mmol) followed by DIPEA (407 mg, 3.147 mmol). The mixture was stirred at room temperature overnight and evaporated. Sodium hydrogencarbonate aqueous solution (sat.) was added into the residue. The mixture was then extracted with ethyl acetate (×2). The extracts were combined and washed with water and brine and dried (magnesium sulphate) and evaporated. Chromatography of the residue on a column (ISOLUTE® SI, 5 g/15 ml) using DCM and then MeOH/DCM (1:99) as eluant gave 265 mg the desired product, yield 77%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07521461B2 |
| 出典データセット | uspto-grants-2009_04 |
| ORD ID | ord-cc98671f87b84a8e8507afecc439120f |
| 出典メモ | uspto-grants-2009_04 |