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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1771861Generated: November 3, 2026

HCID 90420412, compound → HCID 90420305, compound

https://huagongshe.com/reaction/1771861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 90420412HCID 90420412—
ReactantHCID 178418268HCID 178418268—
SolventDichloromethaneHCID 6344—
ProductHCID 90420305HCID 90420305—

Reaction Conditions

Temperature-4 °C

Reaction Steps

A solution of 1-(6-bromo-3-((4-(4-fluorophenyl)thiazol-2-yl)(methyl)amino)imidazo[1,2-a]pyridin-2-yl)-2-phenylethane-1,2-diol (Gen-5-ab) (10.8 g, 20 mmol, 1 eq.) in DCM (500 mL) was cooled to −4° C. Lead tetraacetate (dried before use, 13.3 g, 30 mmol, 1.5 eq.) was added and stirred at −4° C. for 0.5 h. The reaction was quenched by addition of water (500 mL). The mixture was filtered and the layers in the filtrate were separated. The aqueous layer was extracted with DCM (2×200 mL). The combined organic layers were dried over sodium sulfate, filtered and concentrated. The crude product was purified by chromatography on silica gel (elution with heptane/EtOAc 100/0 to 50/50) to give an additional amount of Intermediate Gen-5-q 6-bromo-3-((4-(4-fluorophenyl)thiazol-2-yl)(methyl)amino)imidazo[1,2-a]pyridine-2-carbaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249141B2
Source datasetuspto-grants-2016_02
ORD IDord-3e9d83e1ff874bd6a2b13434b99c57c6
Source noteuspto-grants-2016_02