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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1434671Generated: October 31, 2026

Ammonium Hydroxide → HCID 178527552, compound

https://huagongshe.com/reaction/1434671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AcetateHCID 517045—
Reactant1-Bromo-3-(3,4-dichlorophenyl)propan-2-oneHCID 53403274—
ReactantHCID 85978227HCID 85978227—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 178527552HCID 17852755275.6%

Reaction Steps

To a solution of 1-bromo-3-(3,4-dichloro-phenyl)-propan-2-one (4.1 mmol) in DMF (20 mL) was added sodium acetate (21 mmol) and the mixture was stirred for 2 hr at room temperature before concentrated ammonium hydroxide (5 mL) and ammonium chloride (1 g) were added. After the reaction mixture was stirred for 10 min, 4-(thiazol-2-ylsulfamoyl)-benzamidine (4.1 mmol) was added and the mixture was stirred at 60° C. overnight. After cooled to room temperature, the mixture was diluted with AcOEt (200 mL) and the resulting organic solution was washed with brine, dried over MgSO4, and concentrated in vacuo. The crude product was purified by column chromatography to give 4-[4-(3,4-dichloro-benzyl)-1H-imidazol-2-yl]-N-thiazol-2-yl-benzenesulfonamide (3.1 mmol), which was converted to its sodium salt by reacting with NaOH solution (0.999 N).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615569B2
Source datasetuspto-grants-2009_11
ORD IDord-7eea7505c2d9496ca2a7543eb4adec1d
Source noteuspto-grants-2009_11