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Trifluoroacetic acid → (6-Bromo-pyridazin-3-yl)-(4-chloro-benzyl)-amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Trifluoroacetic acid | HCID 6422 | — |
| 反応物 | 4-Chlorobenzaldehyde | HCID 7726 | — |
| 反応物 | Triethylsilane | HCID 12052 | — |
| 反応物 | 6-Bromopyridazin-3-amine | HCID 2794779 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | (6-Bromo-pyridazin-3-yl)-(4-chloro-benzyl)-amine | HCID 57619288 | — |
反応手順
To 6-bromo-pyridazin-3-ylamine (521, 0.85 g, 0.0049 mol) in acetonitrile (30.0 mL) were added 4-chlorobenzaldehyde (40, 0.82 g, 0.0058 mol), triethylsilane (4.0 mL, 0.025 mol) and trifluoroacetic acid (2.0 mL, 0.026 mol). The reaction was heated to reflux for 4 hours, then poured into water, and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated and washed with ethyl acetate to give a white solid (522, 1.0 g). MS (ESI) [M+H+]+=298.3, 300.2.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08722702B2 |
| 出典データセット | uspto-grants-2014_05 |
| ORD ID | ord-ccf63b55d30f4df48f622b0cd923c1d1 |
| 出典メモ | uspto-grants-2014_05 |