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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039534Generated: November 1, 2026

Acetic Acid → HCID 67042921, compound

https://huagongshe.com/reaction/2039534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 67042814HCID 67042814—
SolventEthyl AcetateHCID 8857—
ProductHCID 67042921HCID 6704292134.2%

Reaction Steps

A mixture of 2-(2-benzo[1,3]dioxol-5-yl-acetylamino)-4-sulfamoyl-benzoic acid (0.10 g, 0.26 mmol), acetic acid (1.5 mL) and acetic anhydride (0.10 mL, 1.06 mmol) was stirred at reflux for 1 h. The reaction was diluted with ethyl acetate and washed with NaHCO3 satured solution, then with water and brine. The organic phase was dried over Na2SO4, filtered and evaporated to give the 2-benzo[1,3]dioxol-5-ylmethyl-4-oxo-4H-benzo[d][1,3]oxazine-7-sulfonic acid amide intermediate (0.032 g) as yellow oil. To a solution of 2-benzo[1,3]dioxol-5-ylmethyl-4-oxo-4H-benzo[d][1,3]oxazine-7-sulfonic acid amide (0.032 g, 0.09 mmol) in dry pyridine (1 mL) was added aminoguanidine hydrogencarbonate (0.013 g, 0.098 mmol) and the mixture was heated under microwave condition at 180° C. for 1.5 h. The solvent was then evaporated and the crude was taken up in methanol to give the title compound (0.013 g, 12% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580783B2
Source datasetuspto-grants-2013_11
ORD IDord-4ca68ed3d1514bf091c4a809cfd2e1d6
Source noteuspto-grants-2013_11