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Benzenepropanoyl chloride → 3-phenyl-N-(2-phenyl-1,3-benzoxazol-5-yl)propanamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzenepropanoyl chloride | HCID 64801 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | 2-Phenyl-1,3-benzoxazol-5-amine | HCID 721059 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 3-phenyl-N-(2-phenyl-1,3-benzoxazol-5-yl)propanamide | HCID 976039 | 75% |
反応手順
To a solution of 2-phenylbenzo[d]oxazol-5-amine (50 mg, 0.24 mmol) in dichloromethane (2 mL) at room temperature was added 3-phenylpropanoyl chloride (44.1 mg, 0.26 mmol) followed immediately by diisopropylethylamine (82 μL, 0.48 mmol). The resulting mixture was stirred at room temperature for 16 h. Dichloromethane was added and the organic layer was washed with saturated aqueous Na2CO3. The combined organic layers were dried over anhydrous MgSO4 and evaporated. The resulting solid was dissolved in methanol, passed through an acidic scavenger column (silica-based quaternary amine SPE-AX from Biotage®) and then evaporated to afford 61.1 mg (75%) of the title compound (LCMS RT=6.45 min, MH+ 343.2)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08518980B2 |
| 出典データセット | uspto-grants-2013_08 |
| ORD ID | ord-03838efeabaa4d9fb9e6abfc63b631db |
| 出典メモ | uspto-grants-2013_08 |