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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492775Generated: October 30, 2026

Phenylacetyl chloride → HCID 57677416, compound

https://huagongshe.com/reaction/492775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyl chlorideHCID 7679—
ReactantPotassium thiocyanateHCID 516872—
ReactantDiethylether hexaneHCID 21584099—
ReactantHCID 23153091HCID 23153091—
SolventAcetonitrileHCID 6342—
ProductHCID 57677416HCID 5767741655%

Reaction Steps

2-Phenylacetyl chloride (0.86 ml) was dissolved in acetonitrile (5 ml) under a nitrogen atmosphere, and then potassium thiocyanate (127 mg) was added thereto at 60° C., followed by stirring at the same temperature for 3 hrs. The reaction mixture was cooled down to room temperature, and then a solution of 4-(4-amino-2-chlorophenoxy)-6-[(pyrrolidin-1-yl)carbonylamino]pyridine (145 mg) in acetonitrile (5 ml) was added thereto, followed by stirring at room temperature for 1.5 hr. The reaction mixture was partitioned between ethyl acetate and a saturated aqueous solution of sodium hydrogencarbonate. The organic layer was washed with a saturated aqueous solution of sodium hydrogencarbonate and brine in this order, and dried over anhydrous sodium sulfate. The solvent was evaporated under a reduced pressure to give a residue, which was then purified by silica gel column chromatography (eluent; hexane:ethyl acetate=1:2). Fractions containing the target compound were concentrated to give a residue, to which diethyl ether/hexane (1/2) was added to suspend. The resultant solid was filtered off and dried under aeration to provide the titled compound (122 mg, 55%) as white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531532B2
Source datasetuspto-grants-2009_05
ORD IDord-35b0215c2ed342418cbf30892632a8a5
Source noteuspto-grants-2009_05