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Sodium Hydroxide → (2S,3S)-3-(5-(1-Cyanocyclopropyl)-2-methoxybenzyl)amino-2-phenylpiperidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 反応物 | 5-(1-Cyanocyclopropyl)-2-methoxybenzaldehyde | HCID 19066432 | — |
| 反応物 | (2S,3S)-2-Phenylpiperidin-3-amine dihydrochloride | HCID 69654807 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (2S,3S)-3-(5-(1-Cyanocyclopropyl)-2-methoxybenzyl)amino-2-phenylpiperidine | HCID 9799042 | 41% |
反応手順
To a stirred suspension of Compound 3 (150 mg, 0.60 mmol) and Compound 2 (145 mg, 0.72 mmol) in dry CH2Cl2 (5 ml) was added NaBH(OAc)3 (358 mg, 1.68 mmol) portionwise at room temperature. The reaction mixture was stirred at room temperature for 6 h. The mixture was basified to pH10-11 with 10% NaOH aq. with ice-cooling. The organic layer was separated and the aqueous layer was extracted with CH2Cl2. The combined solution was washed with brine, dried (MgSO4) and concentrated in vacuo to give crude product. The crude product (300 mg) was purified by column chromatography on silica gel with CH2Cl2 -MeOH (20:1-10:1) to give Compound 4 (89 mg, 41%) as a yellow viscous oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05789423 |
| 出典データセット | uspto-grants-1998_08 |
| ORD ID | ord-eb5d9595d0754a179895ec8f0191ad83 |
| 出典メモ | uspto-grants-1998_08 |