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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017914Generated: October 26, 2026

4-Fluorobenzoyl chloride → 4-Fluoro-N-[3-(4-isopropylphenyl)-1',4,6,7-tetramethylspiro[benzofuran-2(3H),4'-piperidine]-5-yl]benzamide

https://huagongshe.com/reaction/1017914

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzoyl chlorideHCID 67879—
ReactantDiisopropylether methanolHCID 21882575—
Reactant3-(4-Isopropylphenyl)-1',4,6,7-tetramethylspiro[benzofuran-2(3H),4'-piperidine]-5-amineHCID 21961302—
Product4-Fluoro-N-[3-(4-isopropylphenyl)-1',4,6,7-tetramethylspiro[benzofuran-2(3H),4'-piperidine]-5-yl]benzamideHCID 1018540438%

Reaction Steps

By using 3-(4-isopropylphenyl)-1′,4,6,7-tetramethylspiro[benzofuran-2(3H),4′-piperidine]-5-amine and 4-fluorobenzoyl chloride, the title compound was synthesized according to Example 1b. Yield: 38%. Melting point: 271-272° C. (Methanol-isopropyl ether)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479536B1
Source datasetuspto-grants-2002_11
ORD IDord-33988106ccf94bc780a4bf9a2e7df83f
Source noteuspto-grants-2002_11