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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335762Generated: October 25, 2026

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneethanamine, alpha-methyl-, phosphate (1:1)HCID 62885—
ReactantPotassium AcetateHCID 517044—
Reactant2-Bromo-1H-imidazoleHCID 2773261—
Reactant(S)-2'-(neopentyloxy)-7'-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5H-spiro[oxazole-4,9'-xanthen]-2-amineHCID 67246448—
Solvent1-ButanolHCID 263—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product(S)-2'-(1H-imidazol-2-yl)-7'-(neopentyloxy)-5H-spiro[oxazole-4,9'-xanthen]-2-amineHCID 58466116—

Reaction Conditions

Temperature120 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883782B2
Source datasetuspto-grants-2014_11
ORD IDord-813580b86bc541abab42e4b658d2d333
Source noteuspto-grants-2014_11