関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | 5-Methyl-1H-imidazole-4-carbaldehyde | HCID 2795887 | — |
| 反応物 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 反応物 | 1-(5-Chloropyridin-2-yl)-1-(3-fluoro-5-(trifluoromethyl)phenyl)-2-phenylethanamine | HCID 59134573 | — |
| 溶媒 | 1,1-Dichloroethane | HCID 6365 | — |
| 生成物 | HCID 178433274 | HCID 178433274 | 93.8% |
反応手順
To a solution of 1-(5-chloropyridin-2-yl)-1-(3-fluoro-5-(trifluoromethyl)phenyl)-2-phenylethanamine (0.02 g, 0.051 mmol) in dichloroethane (0.5 mL) in a two dram vial was added 4-methyl-1H-imidazole-5-carbaldehyde (6 mg, 0.051 mmol), followed by a drop of acetic acid. The reaction mixture was shaken for 20 minutes at room temperature and then NaBH(OAc)3 was added (12 mg, 0.056 mmol). The reaction was stirred at room temperature overnight. The solvents were removed and the residue was purified by preparative HPLC (phenominex C18 column, 21×100 mm, 5μ) using MeOH/H2O (with 0.1% TFA) to give 1-(5-chloropyridin-2-yl)-1-(3-fluoro-5-(trifluoromethyl)phenyl)-N-((4-methyl-1H-imidazol-5-yl)methyl)-2-phenylethanamine as a white solid (23.4 mg, 76% yield). LCMS: 3.6 min [M+1] 489.2 (4 min gradient, MeOH/H2O 0.1% TFA); 1H NMR (400 MHz, CDCl3) δ ppm 2.27 (s, 3 H), 3.45-3.52 (m, 1 H), 3.88-3.99 (m, 2 H), 4.01-4.07 (m, 1 H), 6.64 (d, J=7.09 Hz, 2 H), 7.02 (d, J=8.56 Hz, 1 H), 7.10 (t, J=7.46 Hz, 2 H), 7.18 (t, J=7.46 Hz, 1 H), 7.49 (d, J=7.58 Hz, 1 H), 7.61 (d, J=9.54 Hz, 1 H), 7.69 (s, 1 H), 7.76 (dd, J=8.56, 2.45 Hz, 1 H), 8.28 (s, 1 H), 8.60 (d, J=1.96 Hz, 1 H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07888376B2 |
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| 出典データセット | uspto-grants-2011_02 |
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| ORD ID | ord-2fa69137c6b14fa0bb181e50dffac910 |
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| 出典メモ | uspto-grants-2011_02 |
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