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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493285Generated: October 31, 2026

Triethylamine → HCID 14726799, compound

https://huagongshe.com/reaction/1493285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-(4-Fluorophenyl)piperazineHCID 75260—
ReactantHCID 14726793HCID 14726793—
SolventTolueneHCID 1140—
ProductHCID 14726799HCID 1472679917.9%

Reaction Conditions

Temperature20 °C

Reaction Steps

The experiment is carried out as in Example 56, starting with 2-(4-bromo-2-butyl)naphtho[1,8-cd]isothiazole 1,1-dioxide (5.2 g), triethylamine (2.1 cc) and 4-(4-fluorophenyl)piperazine (2.8 g) in toluene (200 cc). The mixture is heated at boiling point for 8 hours and 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 a mixture of dichloromethane and ethyl acetate (90-10 as eluant, crystallization from isopropyl oxide (30 cc) and recrystallization from boiling acetonitrile (10 cc), 2-{4-[4-(4-fluorophenyl)-1-piperazinyl]-2butyl)naphtho[1,8-cd]isothiazole 1,1-dioxide (1.2 g) is obtained, m.p. 116° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05021420
Source datasetuspto-grants-1991_06
ORD IDord-6341e94c1ebe4ec2b0f02027b8f3db44
Source noteuspto-grants-1991_06