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Benzyl Bromide → (1R*,2R*,5R*)-8-Benzyl-2-[2,5-bis(trifluoromethyl)phenylmethoxy]-1-phenyl-8-azabicyclo[3.2.1]octane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzyl Bromide | HCID 7498 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 2-(Bromomethyl)-1,4-bis(trifluoromethyl)benzene | HCID 2773199 | — |
| 反応物 | (1R*,2R*,5R*)-8-Benzyl-1-phenyl-8-azabicyclo[3.2.1]octan-2-ol | HCID 69688994 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (1R*,2R*,5R*)-8-Benzyl-2-[2,5-bis(trifluoromethyl)phenylmethoxy]-1-phenyl-8-azabicyclo[3.2.1]octane | HCID 86586657 | — |
反応手順
(1R*,2R*,5R*)-8-Benzyl-1-phenyl-8-azabicyclo[3.2.1]octan-2-ol (Description 9; 151 mg, 0.52 mmol) was treated with sodium hydride (41 mg, 60% in oil, 1.03 mmol) at 0° C. in a solution of THF (2 ml) and allowed to warm to room temperature. The mixture was recooled to 0° C. and 2,5-bis(trifluoromethyl)benzyl bromide (0.24 ml, 1.30 mmol) added and the mixture heated to 50° C. for 2 days. A further 1.30 mmol of the benzyl bromide was added and the mixture further heated for 50° C. for 2 days. The reaction mixture was poured into water and extracted with ethyl acetate (×3), dried (MgSO4) and concentrated in vacuo to give a yellow solid. This was purified by flash column chromatography [25% ethyl acetate in iso-hexane] to give the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06727249B2 |
| 出典データセット | uspto-grants-2004_04 |
| ORD ID | ord-3985ac8dd7a14528a1ab2784fd7fa7cb |
| 出典メモ | uspto-grants-2004_04 |