Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(Bis(4-fluorophenyl)methylene)piperidine | HCID 2724436 | — |
| Reactant | 2(3-Chloropropyl)naphtho[1,8-cd]isothiazole 1,1-dioxide | HCID 14580026 | — |
| Product | HCID 19830852 | HCID 19830852 | — |
Reaction Steps
The experiment is carried out as in Example 1, starting with 2-(3-chloropropyl)naphtho[1,8-cd]isothiazole 1,1-dioxide (3.9 g), triethylamine (1.9 cc), 4-[bis(4-fluorophenyl)methylene]piperidine (3.7 g) and sodium iodide (2.1 g) in toluene (150 cc). The mixture is heated for 6 hours at boiling point, then cooled to a temperature of about 20° C. After purification by flashchromatography on a silica column., under a current of argon at medium pressure (0.5-1.5 bar) with dichloromethene as eluant, 2-(3-[bis(4-fluorophenyl)-4-methylenepiperidino]propyl}naphtho[1,8-cd]-isothiazole 1,1-dioxide (4.6 g) is obtained in the form of a brown oil which is converted to the hydrochloride, m.p. 137° 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-7f91fe0b8ee84803af6a230efec11ab9 |
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| Source note | uspto-grants-1991_06 |
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