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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160772Generated: October 31, 2026

Ethanethiol → 6-Ethylthio-2-trifluoromethylimidazo[1,2-b]pyridazin-3-ylsulfonamide

https://huagongshe.com/reaction/1160772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
Reactant6-Chloro-2-(trifluoromethyl)imidazo[1,2-b]pyridazine-3-sulfonamideHCID 23028108—
ReactantPotassium tert-butoxideHCID 23665647—
Solventtert-ButanolHCID 6386—
Product6-Ethylthio-2-trifluoromethylimidazo[1,2-b]pyridazin-3-ylsulfonamideHCID 23028118—

Reaction Steps

6-Chloro-2-trifluoromethylimidazo[1,2-b]pyridazin-3-ylsulfonamide (1.00 g, 3.33 mmol) was suspended in t-butyl alcohol (20.0 ml) and stirred at room temperature, during which potassium t-butoxide (80%, 1.40 g, 9.98 mmol) and ethanethiol (0.54 ml, 7.29 mmol) were added thereto. After the mixture was heated for 4 hours under reflux, the reaction solution was left and cooled to room temperature, poured into ice-water (200 ml) and adjusted to pH 3. The precipitated crystals were filtered and washed with water to give the title compound as colorless crystals. The yield was 0.54 g (50.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816526B2
Source datasetuspto-grants-2010_10
ORD IDord-2c0ea649e952468daa7124c4237ac838
Source noteuspto-grants-2010_10