関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Bromide ion | HCID 259 | — |
| 反応物 | 2-Bromoacetamide | HCID 69632 | — |
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | (S)-3-Benzyl-1-(3-cyclopentyloxy-4-methoxy-phenyl)-piperazine | HCID 16725642 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (S)-2-(2-benzyl-4-(3-(cyclopentyloxy)-4-methoxyphenyl)piperazin-1-yl)acetamide | HCID 23627744 | — |
反応手順
A solution of the bishydrochloride salt of (S)-3-Benzyl-1-(3-cyclopentyloxy-4-methoxy-phenyl)-piperazine (Example 2) (110 mg, 0.25 mmol) in THF (2 mL) at room temperature was treated with diisopropylethylamine (165 μL, 1.0 mmol) followed by 2-bromoacetamide (42 mg, 0.3 mmol). The reaction mixture was heated at 50° C. for 8 h and an additional amount of bromide (42 mg, 0.3 mmol) then added. The reaction mixture was then stirred for an additional 16 h at room temperature and evaporated. The crude reaction was then partitioned between EtOAc (3 mL) and a saturated aqueous NaHCO3 solution (3 mL). The organic phase was isolated and further washed with an additional portion of a saturated aqueous NaHCO3 solution (3 mL) and brine (2×3 mL).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08501745B2 |
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| 出典データセット | uspto-grants-2013_08 |
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| ORD ID | ord-ce866a58f98c42fbafb114a4d65c4b7a |
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| 出典メモ | uspto-grants-2013_08 |
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