Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 335762생성일: 2026년 10월 26일
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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Benzeneethanamine, alpha-methyl-, phosphate (1:1) | HCID 62885 | — |
| 반응물 | Potassium Acetate | HCID 517044 | — |
| 반응물 | 2-Bromo-1H-imidazole | HCID 2773261 | — |
| 반응물 | (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 | — |
| 용매 | 1-Butanol | HCID 263 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | (S)-2'-(1H-imidazol-2-yl)-7'-(neopentyloxy)-5H-spiro[oxazole-4,9'-xanthen]-2-amine | HCID 58466116 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08883782B2 |
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| 출처 데이터셋 | uspto-grants-2014_11 |
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| ORD ID | ord-813580b86bc541abab42e4b658d2d333 |
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| 출처 메모 | uspto-grants-2014_11 |
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