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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970280Generated: November 3, 2026

1,2-Dimethoxyethane → (S)-2'-bromo-7'-(pyrimidin-5-yl)-5H-spiro[oxazole-4,9'-xanthen]-2-amine

https://huagongshe.com/reaction/1970280

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium CarbonateHCID 10340—
Reactant(Pyrimidin-5-yl)boronic acidHCID 2795193—
Reactant(R)-2'-bromo-7'-iodo-5H-spiro[oxazole-4,9'-xanthen]-2-amineHCID 58466195—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product(S)-2'-bromo-7'-(pyrimidin-5-yl)-5H-spiro[oxazole-4,9'-xanthen]-2-amineHCID 59272310—

Reaction Conditions

Temperature65 °C

Reaction Steps

100 ml RBF was charged with (R)-2′-bromo-7′-iodo-5H-spiro[oxazole-4,9′-xanthen]-2-amine (1.5 g, 3.28 mmol), pyrimidin-5-ylboronic acid (0.488 g, 3.94 mmol), tetrakis(triphenylphosphine)palladium(0) (0.284 g, 0.246 mmol). DME (23.44 mL) followed by sodium carbonate (4.92 mL, 9.85 mmol) (2M solution) were added and the mixture was heated at 65° C. for 24 h. The mixture was diluted with water and EtOAc, filtered and organic layer was separated and concentrated. The crude material was purified by flash chromatography on 40 g RediSep column using 5-70% gradient of DCM/MeOH/NH4OH in DCM to give (S)-2′-bromo-7′-(pyrimidin-5-yl)-5H-spiro[oxazole-4,9′-xanthen]-2-amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426447B2
Source datasetuspto-grants-2013_04
ORD IDord-a6be9390d42a4db18330f2c74d6734f4
Source noteuspto-grants-2013_04