関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-[4-(4-Fluoro-phenoxy)-phenyl]-ethyl-methyl amine | HCID 67774613 | — |
| 反応物 | HCID 178503543 | HCID 178503543 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | HCID 178483269 | HCID 178483269 | 51.2% |
反応手順
2-[4-(4-fluoro-phenoxy)-phenyl]-ethyl-methyl amine (0.204 mmol, 1 eq) and 2-methylsulfanyl-5-pyrimidin-5-ylmethyl-1H-pyrimidin-4-one (0.082 mmol, 0.4 eq) were dissolved in dry ethanol (200 μL) and stirred at 125° C. for 16 hours. Solvent was evaporated and crude product was purified on Biotage SP1 Snap Si 25; 25 ml/min in the gradient of MeOH in DCM: 0-10% in 30CV. The appropriate fractions were combined and evaporated in vacuo to give the required product 2-{2-[4-(4-fluoro-phenoxy)phenyl]-ethyl-methyl-amino}-5-pyrimidin-5-ylmethyl-1H-pyrimidin-4-one (0.042 mmol, yield: 20%, HPLC-MS/UV: [M+H]+=432.14; rt: 10.14 mins; purity: 97%). 1H NMR (300 MHz; CDCl3) δ/ppm 2.89 (t, J=7.17, 2H), 3.59 (s, 2H), 3.69-3.77 (m, 2H), 6.86-7.05 (m, 5H), 7.10-7.18 (m, 2H), 7.23-7.30 (m, 2H), 7.69 (s, 1H), 8.61 (s, 1H), 9.02-9.05 (m, 1H), 9.95 (br.s., 1H)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08637536B2 |
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| 出典データセット | uspto-grants-2014_01 |
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| ORD ID | ord-6ad3b0d5840f4a568878af29314710db |
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| 出典メモ | uspto-grants-2014_01 |
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