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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184925Generated: November 1, 2026

Ammonium Acetate → HCID 22458318, compound

https://huagongshe.com/reaction/2184925

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantHCID 22458356HCID 22458356—
SolventMethanolHCID 887—
ProductHCID 22458318HCID 2245831863.4%

Reaction Steps

To a solution of N-[4-(2-{[(tert-butyl)amino]sulfonyl}phenyl)phenyl][2-(3-cyanophenyl)cyclopent-1-enyl]carboxamide (70 mg, 0.137 mmol) in 5 ml anhydrous methanol cooled in an ice bath was bubbled HCl gas until saturation was achieved. Reaction was allowed to warm to room temperature and stirred overnight. The reaction was then concentrated in vacuo and dried under hi vacuum. The dried residue was dissolved in 5 ml anhydrous methanol to which ammonium acetate (77 mg, 1 mmol) was added and the reaction heated to reflux for 2 hours. The reaction was concentrated and purified on a 2×25 cm Vydac C18 HPLC column to give 3-(2-{N-[4-(2-sulfamoylphenyl)phenyl]carbamoyl}cyclopent-1-enyl)benzenecarboxamidine (40 mg, 63%) as a fluffy white powder after lyophilization. ES-MS (M+H+): 461.15

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06399627B1
Source datasetuspto-grants-2002_06
ORD IDord-16402d90b48142478d7c2d672e41f70e
Source noteuspto-grants-2002_06