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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015426Generated: November 1, 2026

Ammonium thiocyanate → HCID 25096337, compound

https://huagongshe.com/reaction/1015426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium thiocyanateHCID 15666—
Reactant4-Fluorobenzoyl chlorideHCID 67879—
ReactantHCID 67300903HCID 67300903—
SolventAcetoneHCID 180—
ProductHCID 25096337HCID 2509633770%

Reaction Steps

To a stirred solution of 4-fluorobenzoyl chloride (38 mg, 0.24 mmol) in acetone (2.0 mL) was added ammonium thiocyanate (51 mg, 0.66 mmol). The resulting mixture was stirred for 1 h at room temperature followed by the addition of the above-obtained tetrahydroquinoline compound (80 mg, 0.22 mmol). After stirred overnight at room temperature, the reaction mixture was quenched with excess saturated ammonium chloride (20 mL) followed by extraction with ethyl acetate (3×20 L). The organic layers were combined, washed with brine, and then concentrated under vacuum. The residue was purified by silica gel chromatography to give 4-fluoro-N-{5-[5-(naphthalen-1-yloxy)-pentyloxy]-3,4-dihydro-2H-quinoline-1-carbothioyl}-benzamide (83 mg, 0.15 mmol, 70%) as a white solid. MS (EI): m/z 543 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985763B2
Source datasetuspto-grants-2011_07
ORD IDord-74109ca3df184a68bd7192e84aab54d4
Source noteuspto-grants-2011_07