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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500140Generated: October 26, 2026

D-Proline → 2-(4-Bromo-3-fluorophenyl)-7-(4-ethoxyphenoxy)imidazo[1,2-b][1,2,4]triazine

https://huagongshe.com/reaction/500140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantD-ProlineHCID 8988—
ReactantChlorosuccinimideHCID 31398—
ReactantAcetaldehyde, (4-methoxyphenoxy)-HCID 96383—
Reactant6-(4-Bromo-3-fluorophenyl)-1,2,4-triazin-3-amineHCID 57516523—
SolventChloroformHCID 6212—
Product2-(4-Bromo-3-fluorophenyl)-7-(4-ethoxyphenoxy)imidazo[1,2-b][1,2,4]triazineHCID 68462474—

Reaction Steps

To a cooled (0° C.) mixture of (4-methoxyphenoxy)acetaldehyde (33.2 mg, 0.2 mmol) and D-proline (4.6 mg, 0.04 mmol) in chloroform (1.0 mL) was added N-chlorosuccinimide (26.7 mg, 0.2 mmol) with stirring. The mixture was stirred at 0° C. for 30 min, then gradually warmed to ambient temperature for 2 h. To the reaction mixture was added 6-(4-bromo-3-fluorophenyl)-1,2,4-triazin-3-amine (26.9 mg, 0.1 mmol). The reaction mixture was stirred for 1 h and then the solvent was removed under reduced pressure. The residue was dissolved in isopropanol (2 mL) and heated to 100° C. overnight. After cooling, the mixture was filtered and the filtrate was purified by RP-HPLC (pH 10) to afford the desired product. LCMS: (M+H)=415.0/416.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767675B2
Source datasetuspto-grants-2010_08
ORD IDord-fd2f9702dba042d9bf06fb42361ac3e2
Source noteuspto-grants-2010_08