Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484448Generated: October 27, 2026

Ammonium Hydroxide → 6-Chloroimidazo[2,1-b][1,3]thiazole-5-sulfonamide

https://huagongshe.com/reaction/1484448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant6-Chloroimidazo(2,1-b)(1,3)thiazole-5-sulfonyl chlorideHCID 2799717—
SolventAcetonitrileHCID 6342—
Product6-Chloroimidazo[2,1-b][1,3]thiazole-5-sulfonamideHCID 277983988%

Reaction Conditions

Temperature0 °C

Reaction Steps

2 g (1 mol equiv.) 6-Chloro-imidazo[2,1-b]thiazole-5-sulfonyl chloride was dissolved in 20 mL acetonitrile and cooled to 0° C. Dropwise, 3.7 mL (3 mol equiv.) ammoniumhydroxide was added and the reaction mixture was stirred at room temperature for 10 min, during which a white precipitate was formed. Volatiles were removed under reduced pressure, and the solid residue was washed with water and dried in vacuo affording 1.62 g (88%) 6-chloro-imidazo[2,1-b]thiazole-5-sulfonic acid amide. 1H NMR (400 MHz, DMSO-d6) δ 7.62 (d, J=4.6 1H), 7.98 (d, J=4.6 Hz, 1H), 8.00 (br.s., 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422244B2
Source datasetuspto-grants-2016_08
ORD IDord-d8153386d03442679950960c59e5a202
Source noteuspto-grants-2016_08