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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087500Generated: November 1, 2026

Triethylamine → HCID 15710728, compound

https://huagongshe.com/reaction/1087500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-(2-Fluorophenyl)piperazineHCID 70529—
Reactant2(3-Chloropropyl)naphtho[1,8-cd]isothiazole 1,1-dioxideHCID 14580026—
SolventTolueneHCID 1140—
ProductHCID 15710728HCID 1571072846.2%

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 (7 g), triethylamine (3.5 cc) and 4-(2-fluorophenyl)piperazine (4.4 g) in toluene (150 cc). The mixture is heated for 8 hours at boiling point, then cooled to a temperature of about 20° C. After purification by flash-chromatography on a silica column, under a current of argon at medium pressure (0.5-1.5 bar) with dichloromethane as eluant, and recrystallization from boiling acetonitrile (15 cc), 2-{3-[4-(2-fluorophenyl)-1-piperazinyl]propyl)naphtho[1,8-cd]isothiazole 1,1dioxide (4.8 g) is obtained, m.p. 112° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05036075
Source datasetuspto-grants-1991_07
ORD IDord-33a8730730ff489293ac223b0701b7c5
Source noteuspto-grants-1991_07