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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095991Generated: November 1, 2026

Iodine → HCID 68743737, compound

https://huagongshe.com/reaction/2095991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPotassium CarbonateHCID 11430—
ReactantN1-Methyl-1-phenylethylenediamineHCID 98060—
Reactant1-[[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl]-4-[4-(5-phenyl-3-isoxazolyl)-2-thiazolyl]piperidineHCID 68742226—
ReactantHCID 86631244HCID 86631244—
Solventtert-ButanolHCID 6386—
ProductHCID 68743737HCID 68743737—

Reaction Steps

To a solution of 4-(4-formyl-2-thiazolyl)-1-[[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl]piperidine (i.e. the product of Example 2, Step B) (0.8 g, 2.07 mmol) in tert-butanol (5 mL) was added N1-methyl-1-phenyl-1,2-ethanediamine (43.57 mg, 0.29 mmol). The reaction mixture was stirred at room temperature under a nitrogen atmosphere for 30 minutes, and then potassium carbonate (107.8 mg, 0.78 mmol) and iodine (43.57 mg, 0.33 mmol) were added. The reaction mixture was stirred at 70° C. for 3 h and then quenched by addition of saturated aqueous sodium sulfite solution until the iodine color almost disappeared. The reaction mixture was extracted with chloroform, and the organic layer was washed with saturated aqueous sodium bicarbonate solution and brine, dried (Na2SO4), filtered and concentrated. The residue was purified by preparative thin-layer chromatography on silica gel using a mixture of 94% ethyl acetate, 5% methanol and 1% triethylamine as eluant to give 64 mg of the title product as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08449898B2
Source datasetuspto-grants-2013_05
ORD IDord-fef34ff316314e6abcb093c4f2f4705b
Source noteuspto-grants-2013_05