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2,6-Dibromopyridine → 1-(6-Bromopyridin-2-yl)pyrrolidin-3-ol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2,6-Dibromopyridine | HCID 12274 | — |
| 反応物 | 4-Hydroxypyrrolidine | HCID 98210 | — |
| 反応物 | Undec-4-ene | HCID 136496 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 1-(6-Bromopyridin-2-yl)pyrrolidin-3-ol | HCID 21942298 | — |
反応手順
A mixture of 2,6-dibromopyridine (2.37 g, 0.01 mol), pyrrolidin-3-ol (1.0 g, 0.01 mol), 1,8-diazabicclo[5.4.0)-7-undecene (1.5 mL) in 10 mL of THF was heated at 70° C. under a nitrogen atmosphere for 11 hours. The reaction mixture was then cooled to room temperature, diluted with ethyl acetate (30 mL). The resulting solution was washed with water and brine, dried over anhydrous magnesium sulfate, filtered and concentrated. The residue was purified by silica gel chromatography (10-30% ethyl acetate/hexane) to give the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08367706B2 |
| 出典データセット | uspto-grants-2013_02 |
| ORD ID | ord-23d8af70e5b34017a33c984f345e567d |
| 出典メモ | uspto-grants-2013_02 |