HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015426Generated: November 1, 2026
Ammonium thiocyanate → HCID 25096337, compound
https://huagongshe.com/reaction/1015426
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium thiocyanate | HCID 15666 | — |
| Reactant | 4-Fluorobenzoyl chloride | HCID 67879 | — |
| Reactant | HCID 67300903 | HCID 67300903 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 25096337 | HCID 25096337 | 70% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07985763B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-74109ca3df184a68bd7192e84aab54d4 |
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| Source note | uspto-grants-2011_07 |
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