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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484141Generated: October 29, 2026

Bromide ion → HCID 10501072, compound

https://huagongshe.com/reaction/484141

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(4-Bromobutyl)-4-thiazolidinoneHCID 10847505—
Reactant3-(Piperazin-1-yl)isoquinolineHCID 13025569—
ReactantDichloromethane methanolHCID 21226129—
SolventAcetonitrileHCID 6342—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 10501072HCID 10501072—

Reaction Conditions

Temperature75 °C

Reaction Steps

A mixture of 3-(4-bromobutyl)-4-thiazolidinone (4.00 g), 1-(3-isoquinolinyl)piperazine (3.53 g), K2CO3 (6.22 g), NaI (300 mg) and acetonitrile (190 mL) was heated at 75° C. (bath temperature) under N2. After 16 h, TLC analysis (silica gel, 40% EtOAc/hexane) showed the absence of starting bromide and a major product at Rf =0.22 (silica gel, 5% MeOH/CH2Cl2). The reaction mixture was cooled to ambient temperature and filtered, the inorganic solid was washed with hot ethyl acetate, and the wash was combined with the above filtrate and concentrated in vacuo to a green solid. The solid was triturated with hot ethyl acetate (300 mL) and the mixture filtered. The filtrate was concentrated in vacuo to a solid which was chromatographed (Waters Prep 500, 1 silica gel column, 5% MeOH/CH2Cl2) to yield 5.10 g of a green solid. The solid was recrystallized from methylene chloride/hexanes to give 2.99 g of light green crystals, mp 145°-146.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05229388
Source datasetuspto-grants-1993_07
ORD IDord-0e71e649a18f4fbfade18e370ba4e24d
Source noteuspto-grants-1993_07