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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087499Generated: October 31, 2026

Triethylamine → HCID 15710729, compound

https://huagongshe.com/reaction/1087499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-(3-Fluorophenyl)piperazineHCID 77418—
Reactant2(3-Chloropropyl)naphtho[1,8-cd]isothiazole 1,1-dioxideHCID 14580026—
SolventTolueneHCID 1140—
ProductHCID 15710729HCID 1571072937.6%

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 (8.4 g), triethylamine (4.2 cc) and 4-(3-fluorophenyl)piperazine (5.3 g) in toluene (100 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 I current of argon at medium pressure (0.5-1.5 bar) with dichloromethane and then a mixture of dichloromethane and ethyl acetate (50-50 vol) as eluant, and recrystallization from boiling acetonitrile (20 cc), 2-{3-[4-(3-fluorophenyl)-1-piperazinyl]propyl)naphtho[1,8-cd]isothiazole 1,1-dioxide (4.7 g) is obtained, m.p. 103° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05036075
Source datasetuspto-grants-1991_07
ORD IDord-ae8f0aa76b7848b68f0871b6a7e49dec
Source noteuspto-grants-1991_07