Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970313Generated: November 4, 2026

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

https://huagongshe.com/reaction/1970313

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

Temperature70 °C

Reaction Steps

A 100 ml RBF was charged with (R)-2′-bromo-7′-iodo-5H-spiro[oxazole-4,9′-xanthen]-2-amine (3.3 g, 7.22 mmol), pyrimidin-5-ylboronic acid (1.163 g, 9.39 mmol), and tetrakis(triphenylphosphine)palladium(0) (0.834 g, 0.722 mmol). To this were added DME (51.6 mL) followed by sodium carbonate (10.83 mL, 21.66 mmol) (2M solution) and the mixture was heated at 70° C. for 24 hrs. The mixture was diluted with water and ethyl acetate, filtered and organic layer was separated and concentrated. The crude material was purified by FC on 80 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-1c62fc14217d4aac87b6c64c3a51023e
Source noteuspto-grants-2013_04