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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772260Generated: November 2, 2026

Potassium Carbonate → HCID 86719495, compound

https://huagongshe.com/reaction/1772260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 86719494HCID 86719494—
ReactantHCID 86719496HCID 86719496—
SolventAcetonitrileHCID 6342—
ProductHCID 86719495HCID 8671949541.7%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 1-[(5-chloro-2,3-dihydro-1-benzofuran-2-yl)methyl]-4-(2-chloroethyl)piperazine (200 mg, 0.61 mmol) in acetonitrile (5 ml) was added potassium carbonate (139 mg, 1.01 mmol, 1.6 eq.), 4-[4-nitro-3-(trifluoromethyl)phenyl]aminophenol (200 mg, 0.67 mmol, 1.1 eq.) and KI (56 mg, 0.34 mmol, 0.6 eq.) with stirring for 3 hours at 70° C. (oil bath). The reaction mixture was concentrated under vacuum to give a residue, which was purified by silica gel column chromatography using 2% dichloromethane in methanol to afford 1-[4-[(5-chloro-2,3-dihydro-1-benzofuran-2-yl)methyl]piperazin-1-yl]-2-(4-[[4-nitro-3-(trifluoromethyl)phenyl]amino]phenoxy)ethan-1-one as a orange solid (150.3 mg, 36%); (ES, m/z): [M+H]+ 591.15; 1H NMR (300 MHz, CDCl3): δ 7.98 (d, J=9.0 Hz, 1H), 6.91-7.11 (m, 4H), 7.08 (d, J=8.7 Hz, 1H), 7.01 (d, J=8.7 Hz, 2H), 6.92 (dd, J=2.7, 9.0 Hz, 1H), 6.69 (d, J=8.4 Hz, 1H), 6.32 (s, 1H), 4.93-5.09 (m, 1H), 4.75 (s, 2H), 3.65-3.78 (m, 4H), 3.28 (dd, J=9.3, 15.9 Hz, 1H), 2.97 (dd, J=8.1, 15.6 Hz, 1H), 2.79 (dd, J=7.5, 13.5 Hz, 1H), 2.60-2.75 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249102B2
Source datasetuspto-grants-2016_02
ORD IDord-f48de476fd9d45b1924525f8deba409a
Source noteuspto-grants-2016_02