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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696784Generated: November 1, 2026

Acetic Anhydride → HCID 67273906, compound

https://huagongshe.com/reaction/1696784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 178503297HCID 178503297—
ProductHCID 67273906HCID 67273906—

Reaction Steps

A solution of 0.094 g 6-Amino-N-hydroxy-4-methylsulfanyl-pyridine-2-carboxamidine in 1.5 ml acetic acid anhydride was heated to reflux for 6 h. The solvent was evaporated and the solidifying residue was taken up in 1.5 ml 1N hydrochloric acid and heated to reflux for 1 h. The reaction mixture was partitioned between 2 ml 1N aqueous sodium hydroxide and ethyl acetate. The phases were separated and the organic phase was washed with water and brine dried over magnesium sulfate and evaporated. The residue triturated in ethyl acetate (1 ml) and the resulting solid was collected by filtration to yield 0.057 g of the title compound as light yellow solid MS (ISP) M+H+=223.3

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163778B2
Source datasetuspto-grants-2012_04
ORD IDord-533634cd030d434998cfbd0ec7613361
Source noteuspto-grants-2012_04