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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835113Generated: October 25, 2026

3-(2-Bromoethyl)indole → 3-(2-Bromoethyl)-1-(6-chloroimidazo[2,1-b]thiazole-5-sulfonyl)indole

https://huagongshe.com/reaction/1835113

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(2-Bromoethyl)indoleHCID 76924—
Reactant6-Chloroimidazo(2,1-b)(1,3)thiazole-5-sulfonyl chlorideHCID 2799717—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product3-(2-Bromoethyl)-1-(6-chloroimidazo[2,1-b]thiazole-5-sulfonyl)indoleHCID 1125934958%

Reaction Steps

A mixture of 3-(2-bromoethyl)indole (1.0 g, 4.46 mmol) and 6-chloroimidazo[2,1-b]thiazole-5-sulfonyl chloride (0.96 g, 1.1 eq.) in THF is treated with potassium t-butoxide (0.48 g, 1.1 equiv.) at room temperature, stirred for 16 h, quenched with saturated NaHCO3 and extracted with EtOAc. The extracts are combined, dried over MgSO4 and concentrated in vacuo to give the title product as a brown oil, 1.2 g (58% yield), identified by HPLC and mass spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770642B2
Source datasetuspto-grants-2004_08
ORD IDord-1c31d52117e2466ea1e8d202eb25264e
Source noteuspto-grants-2004_08