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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184915Generated: November 1, 2026

Ethyl Acetate → HCID 44284734, compound

https://huagongshe.com/reaction/2184915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium AcetateHCID 517165—
ReactantHCID 70097558HCID 70097558—
SolventMethanolHCID 887—
ProductHCID 44284734HCID 44284734—

Reaction Steps

To a solution of (2E)-N-[4-(2-{[(tert-butyl)amino]sulfonyl}phenyl)phenyl]-3-(3-cyanophenyl)-4-methoxybut-2-enamide (150 mg, 0.298 mmol) in 10 ml 1:1 ethyl acetate:anhydrous methanol cooled to −78° C. 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 methyl imidate 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, treated with trifluoroacetic acid (10 ml) for 2 hrs, concentrated and purified on a 2×25 cm Vydac C18 HPLC column to give 3-((1E)-1-(methoxymethyl)-2-{N-[4-(2-sulfamoylphenyl)phenyl]carbamoyl}vinyl)benzenecarboxamidine (34 mg, (25%) as a fluffy off-white powder after lyophilization. ES-MS (M+H+): 465.15

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06399627B1
Source datasetuspto-grants-2002_06
ORD IDord-a4910f19cfce4649aa60bd6026ba943e
Source noteuspto-grants-2002_06