Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787046Generated: October 30, 2026

Ethyl Acetate → HCID 86615783, compound

https://huagongshe.com/reaction/1787046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86615782HCID 86615782—
SolventTetrahydrofuran 2-propanolHCID 22597222—
ProductHCID 86615783HCID 8661578390.7%

Reaction Steps

To a solution of N-(4-{[3-chloro-4-(3-cyanophenoxy)phenyl]amino}-6-iodopyrimidin-5-yl)-2,2,2-trifluoro-N-methylacetamide (1.0 g) in isopropanol-tetrahydrofuran (5.0 mL-10 mL) was added sodium borohydride (70 mg) at room temperature. The mixture was stirred at room temperature for 1.5 hrs, and ethyl acetate was added. The mixture washed with water and saturated brine and the organic layer was dried over magnesium sulfate. After concentration under reduced pressure, the residue was separated and purified by silica gel column chromatography (eluent, hexane:ethyl acetate=4:1→3:2) to give the title compound (755 mg) as a white amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507740B2
Source datasetuspto-grants-2009_03
ORD IDord-ecf93b431f3f4e69b4a56b01fcadb82b
Source noteuspto-grants-2009_03