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2-Amino-3-benzyloxypyridine → 8-(Benzyloxy)-2-(4-fluorophenyl)imidazo[1,2-a]pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Amino-3-benzyloxypyridine | HCID 90334 | — |
| 反応物 | 2-Bromo-1-(4-fluorophenyl)ethan-1-one | HCID 96749 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 8-(Benzyloxy)-2-(4-fluorophenyl)imidazo[1,2-a]pyridine | HCID 18436714 | 25% |
反応手順
3-(Benzyloxy)pyridin-2-amine (2.52 g, 13 mmol) and 2-bromo-1-(4-fluorophenyl)ethanone (2.73 g, 13 mmol) in ethanol (30 mL) were heated at 75° C. for 16 hours. The mixture was concentrated and the residue was purified by silica gel chromatography, eluting with dichloromethane and then 10% methanol in dichloromethane to yield 1.03 g (25%) of 8-(benzyloxy)-2-(4-fluorophenyl)imidazo[1,2-a]pyridine. 1H NMR (CDCl3): δ 8.01 (dd, 2H), 7.82 (s, 1H), 7.78 (d, 1H), 7.55 (d, 2H), 7.41 (m, 3H), 7.14 (t, 2H), 6.65 (t, 1H), 6.48 (d, 1H), 5.44 (s, 2H); MS m/z 319 (M+1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07186714B2 |
| 出典データセット | uspto-grants-2007_03 |
| ORD ID | ord-03c940d437dd4037a5e45c29490526e4 |
| 出典メモ | uspto-grants-2007_03 |