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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

반응식

참여 물질

역할이름HCID투입량
반응물Benzeneethanamine, alpha-methyl-, phosphate (1:1)HCID 62885—
반응물Potassium AcetateHCID 517044—
반응물2-Bromo-1H-imidazoleHCID 2773261—
반응물(S)-2'-(neopentyloxy)-7'-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5H-spiro[oxazole-4,9'-xanthen]-2-amineHCID 67246448—
용매1-ButanolHCID 263—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물(S)-2'-(1H-imidazol-2-yl)-7'-(neopentyloxy)-5H-spiro[oxazole-4,9'-xanthen]-2-amineHCID 58466116—

반응 조건

온도120 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08883782B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-813580b86bc541abab42e4b658d2d333
출처 메모uspto-grants-2014_11