関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | 4-nitro-1H-pyrazole | HCID 16376 | — |
| 反応物 | (S)-tert-butyl 2-((methylsulfonyloxy)methyl)morpholine-4-carboxylate | HCID 86673567 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | (S)-tert-butyl 2-((4-nitro-1H-pyrazol-1-yl)methyl)morpholine-4-carboxylate | HCID 118023401 | 107.7% |
反応手順
To a solution of (S)-tert-butyl 2-((methylsulfonyloxy)methyl)morpholine-4-carboxylate (2.8 g, 9.5 mmol) and 4-nitro-1H-pyrazole (715 mg, 6.3 mmol) in acetonitrile (100 mL) was added cesium carbonate (6.2 g, 19.0 mmol). The reaction mixture was stirred at 55° C. overnight and then concentrated. The residue was dissolved in ethyl acetate (100 mL), washed with water (50 mL), dried over sodium sulfate, filtered and concentrated. The crude sample was purified by silica gel chromatography, eluting with petroleum ether:ethyl acetate=8:1, to afford (S)-tert-butyl 2-((4-nitro-1H-pyrazol-1-yl)methyl)morpholine-4-carboxylate as a yellow oil (2.12 g, 71%). MS (ES+) C13H20N4O5 requires: 312, found: 257 [M+H-56]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09334263B2 |
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| 出典データセット | uspto-grants-2016_05 |
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| ORD ID | ord-569ae0dfd35e4a7a8fd5e1dd96f9ab2f |
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| 出典メモ | uspto-grants-2016_05 |
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