Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483433Generated: October 25, 2026

Water → HCID 19752300, compound

https://huagongshe.com/reaction/483433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant1-(4-Aminobutyl)-4-(2-methoxyphenyl)piperazineHCID 10999903—
ReactantBenzo[d]isothiazole-3-carbonyl chlorideHCID 15639471—
SolventTolueneHCID 1140—
ProductHCID 19752300HCID 1975230069.4%

Reaction Steps

A mixture of 1,2-benzisothiazole-3-carboxylic acid chloride (2.44 g), 1-(2-methoxyphenyl)-4-(4-aminobutyl)piperazine (3.26 g), and triethylamine (6 ml), in sieve-dried toluene (100 ml) was heated to 80° C., with stirring, overnight. After 24 hr, the reaction mixture was cooled to room temperature and poured into water. The organic phase was separated and the aqueous phase was extracted with ether. The ether extracts and toluene phase were combined, dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated in vacuo. The residue was chromatographed on silica using ethyl acetate as the eluent. The appropriate fractions were collected and concentrated. The residue was taken up in ether and ethereal hydrogen chloride was added. The precipitate was recrystallized from ethanol/ethyl acetate and dried (0.1 mm mercury, refluxing toluene temperature) to provide 2.13 g (34.6%) of product, mp 175°-178° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05225412
Source datasetuspto-grants-1993_07
ORD IDord-c66bb03bcf30429b82dd13dd0901cfb0
Source noteuspto-grants-1993_07