HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492775Generated: October 30, 2026
Phenylacetyl chloride → HCID 57677416, compound
https://huagongshe.com/reaction/492775
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Reactant | Diethylether hexane | HCID 21584099 | — |
| Reactant | HCID 23153091 | HCID 23153091 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 57677416 | HCID 57677416 | 55% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07531532B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-35b0215c2ed342418cbf30892632a8a5 |
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| Source note | uspto-grants-2009_05 |
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