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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422172Generated: November 1, 2026

Trifluoroacetic anhydride → HCID 86649145, compound

https://huagongshe.com/reaction/2422172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 86649146HCID 86649146—
SolventPyridineHCID 1049—
ProductHCID 86649145HCID 86649145100%

Reaction Steps

To a solution of N-(4-{([5-(2-amino-2-oxoethyl)-4-chloro-6-(dimethylamino)pyrimidin-2-yl]methyl}phenyl)-2-naphthamide (0.360 g, 0.76 mmol) in pyridine (15 mL) at rt was added trifluoroacetic anhydride (0.161 mL, 1.14 mmol) dropwise and the resulting reaction mixture was stirred at room temperature for 15 hours. The volatiles were removed in vacuo and the remaining residue was partitioned between EtOAc and saturated aqueous ammonium chloride solution. The separated organic layer was washed with brine, dried over anhydrous Na2SO4, filtered, and concentrated in vacuo. Purification of the resulting crude product by silica gel chromatography eluting with 20% EtOH in CHCl3 gave N-(4-{([4-chloro-5-(cyanomethyl)-6-(dimethylamino)pyrimidin-2-yl]methyl}phenyl)-2-naphthamide as an amorphous solid (0.345 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960393B2
Source datasetuspto-grants-2011_06
ORD IDord-6ab7e85e3a6544c5b71238d996a5f7b4
Source noteuspto-grants-2011_06