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HRID 522629作成日:2026年10月27日

Cesium carbonate → (S)-tert-butyl 2-((4-nitro-1H-pyrazol-1-yl)methyl)morpholine-4-carboxylate

https://huagongshe.com/reaction/522629

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物4-nitro-1H-pyrazoleHCID 16376—
反応物(S)-tert-butyl 2-((methylsulfonyloxy)methyl)morpholine-4-carboxylateHCID 86673567—
溶媒AcetonitrileHCID 6342—
生成物(S)-tert-butyl 2-((4-nitro-1H-pyrazol-1-yl)methyl)morpholine-4-carboxylateHCID 118023401107.7%

反応条件

温度55 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US09334263B2
出典データセットuspto-grants-2016_05
ORD IDord-569ae0dfd35e4a7a8fd5e1dd96f9ab2f
出典メモuspto-grants-2016_05