HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493264Generated: October 31, 2026
Potassium Carbonate → HCID 19830855, compound
https://huagongshe.com/reaction/1493264
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,2,3,6-Tetrahydro-4-phenylpyridine | HCID 82553 | — |
| Reactant | HCID 14580047 | HCID 14580047 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 19830855 | HCID 19830855 | 32.1% |
Reaction Steps
5-Acetylamino-2-(3-chloropropyl)naphto[1,8-cd]isothiazole 1,1-dioxide (0.8 g), 4-phenyl-1,2,3,6-tetrahydropyridine (0.4 g), potassium carbonate (4 g) and acetonitrile (25 cc) are heated at boiling point for 20 hours. The reaction mixture is cooled to a temperature of about 20° C. The solution is filtered and then concentrated to dryness at 40° C. under reduced pressure (20 mm Hg; 2.7 kPa). The residue is purified by chromatography on a silica column with a mixture of ethyl acetate and methylene chloride (70-30 vol) as eluant, then recrystallized from boiling ethanol (20 cc). 5Acetylamino-2-[3-(4-phenyl 1,2,3,6-tetrahydro-1-pyridyl)-propyl]naphtho[1,8-cd]isothiazole 1,1-dioxide (0.35 g) is obtained, m.p. 178° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05021420 |
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| Source dataset | uspto-grants-1991_06 |
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| ORD ID | ord-898407cf227f46dab571852d1dc393f3 |
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| Source note | uspto-grants-1991_06 |
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