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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493263Generated: October 31, 2026

Toluene → HCID 19830852, compound

https://huagongshe.com/reaction/1493263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium IodideHCID 5238—
ReactantTriethylamineHCID 8471—
Reactant4-(Bis(4-fluorophenyl)methylene)piperidineHCID 2724436—
Reactant2(3-Chloropropyl)naphtho[1,8-cd]isothiazole 1,1-dioxideHCID 14580026—
ProductHCID 19830852HCID 19830852—

Reaction Conditions

Temperature20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05021420
Source datasetuspto-grants-1991_06
ORD IDord-7f91fe0b8ee84803af6a230efec11ab9
Source noteuspto-grants-1991_06