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HRID 335762作成日:2026年10月26日
Benzeneethanamine, alpha-methyl-, phosphate (1:1) → (S)-2'-(1H-imidazol-2-yl)-7'-(neopentyloxy)-5H-spiro[oxazole-4,9'-xanthen]-2-amine
https://huagongshe.com/reaction/335762
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzeneethanamine, alpha-methyl-, phosphate (1:1) | HCID 62885 | — |
| 反応物 | Potassium Acetate | HCID 517044 | — |
| 反応物 | 2-Bromo-1H-imidazole | HCID 2773261 | — |
| 反応物 | (S)-2'-(neopentyloxy)-7'-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5H-spiro[oxazole-4,9'-xanthen]-2-amine | HCID 67246448 | — |
| 溶媒 | 1-Butanol | HCID 263 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | (S)-2'-(1H-imidazol-2-yl)-7'-(neopentyloxy)-5H-spiro[oxazole-4,9'-xanthen]-2-amine | HCID 58466116 | — |
反応手順
A solution of (S)-2′-(neopentyloxy)-7′-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5H-spiro[oxazole-4,9′-xanthen]-2-amine (50 mg, 0.108 mmol) in BuOH (861 μL), 2-bromo-1H-imidazole (0.129 mmol), and KOAc (31.7 mg, 0.323 mmol) in Water (215 μL) was purged with Ar in a sealed tube. AmPhos (1.525 mg, 2.153 μmol) was added and the reaction was heated to 120° C. for 30 min in the microwave. The reaction was cooled to rt, diluted with MeOH (3 ml), loaded onto an AccuBOND II SCX cartridge, washed with MeOH (3 ml) and eluted with 2N NH3 in MeOH (6 ml) to give the crude product which was purified by reverse-phase preparative HPLC using a Gemini NX c!8 column (150*30 mm, 5 um), 0.1% TFA in CH3CN/H2O, gradient 0% to 70% over 10 min to provide (S)-2′-(1H-imidazol-2-yl)-7′-(neopentyloxy)-5H-spiro[oxazole-4,9′-xanthen]-2-amine.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08883782B2 |
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| 出典データセット | uspto-grants-2014_11 |
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| ORD ID | ord-813580b86bc541abab42e4b658d2d333 |
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| 出典メモ | uspto-grants-2014_11 |
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