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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2036800Generated: November 2, 2026

Chloroacetone → HCID 67055861, compound

https://huagongshe.com/reaction/2036800

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetoneHCID 6571—
ReactantHCID 62148617HCID 62148617—
SolventEthanolHCID 702—
ProductHCID 67055861HCID 6705586166%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 2-amino-5-bromo-N-tert-butylpyridine-3-sulfonamide (3.0 g, 9.7 mmol) in ethanol (6 mL) was added chloroacetone (3.0 mL, 48 mmol) and the reaction mixture was stirred at 80° C. for 48 h. The solvents were evaporated under reduced pressure and the residue was purified by flash silica gel column chromatography (5% methanol in DCM) to yield 6-bromo-N-tert-butyl-2-methylimidazo[1,2-a]pyridine-8-sulfonamide (2.2 g, 66%), which was used without further purification. LCMS Method T: retention time 1.33 min; [M+1]=346.64.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575184B2
Source datasetuspto-grants-2013_11
ORD IDord-7a387e572f88485ca3fb25a2df2736da
Source noteuspto-grants-2013_11