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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245709Generated: October 30, 2026

Cyanuric chloride → HCID 59216379, compound

https://huagongshe.com/reaction/2245709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanuric chlorideHCID 7954—
ReactantHCID 59216414HCID 59216414—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59216379HCID 5921637997.7%

Reaction Steps

To a suspension of 1.3 g of 2-[2-(4-Methoxy-benzyl)-1-oxo-1,2,3,4-tetrahydro-isoquinolin-6-yl]-acetamide in 5 mL of THF and 10 mL of DMF was added 370 mg of cyanuric chloride and after stirring at room temperature for 0.5 hour, the reaction mixture was partitioned between ethyl acetate and brine. The organic layer was washed with 5% sodium bicarbonate, followed by brine and then dried over sodium sulfate. Purification by flash chromatograpy on silica gel column using 75% ethyl acetate in hexane as eluent afforded 1.2 g of [2-(4-Methoxy-benzyl)-1-oxo-1,2,3,4-tetrahydro-isoquinolin-6-yl]-acetonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07683064B2
Source datasetuspto-grants-2010_03
ORD IDord-ccac4c0d69974a6abc2a7d202c6d3216
Source noteuspto-grants-2010_03