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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087487Generated: October 29, 2026

Triethylamine → HCID 14580038, compound

https://huagongshe.com/reaction/1087487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-(4-Bromophenyl)piperazineHCID 2735629—
Reactant2(3-Chloropropyl)naphtho[1,8-cd]isothiazole 1,1-dioxideHCID 14580026—
SolventTolueneHCID 1140—
ProductHCID 14580038HCID 1458003844.5%

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 (5.6 g), triethylamine (2.8 cc) and 4-(4-bromophenyl)piperazine (4.8 g) in toluene (60 cc). The mixture is heated for 8 hours at boiling point, then cooled to a temperature of about 20° C. Stirring is continued for 8 hours at this temperature. After purification by flash-chromatography on a silica column, under a current of argon at medium pressure re (0.5-1.5 bar) with ethyl acetate as eluant, and recrystallization from boiling acetonitrile (40 cc), 2-{3-[4-(4-bromophenyl)-1-piperazinyl]propyl)naphtho[1,8-cd]isothiazole 1,1-dioxide (4.3 g) is obtained, m.p. 149° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05036075
Source datasetuspto-grants-1991_07
ORD IDord-a130f66308ed494d8de9841fbbd7506f
Source noteuspto-grants-1991_07