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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734961Generated: November 4, 2026

Acetic Anhydride → HCID 57843254, compound

https://huagongshe.com/reaction/734961

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSulfuryl chlorideHCID 24648—
ReactantHCID 68506108HCID 68506108—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
SolventSodium BicarbonateHCID 516892—
ProductHCID 57843254HCID 5784325458.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 5-[3-(4-methyl-1-piperazinyl)-6-quinoxalinyl]-2-pyridinamine (0.46 mmol) in pyridine (3 ml) was treated with a sulfonyl chloride, acyl chloride or anhydride such as acetic anhydride (0.56 mmol) and heated at 50° C. for 18 hour. The reaction mixture was treated with another portion of acetic anhydride (0.10 mmol) and stirred for another 2 days. The reaction mixture was diluted with water and saturated sodium bicarbonate (aq) and extracted with ethyl acetate. The ethyl acetate layer was dried over Na2SO4 filtered and concentrated under reduced pressure. The residue was taken into hot ethyl acetate and diluted with hexanes and cool to 0° C. The reaction mixture was filtered and washed with hexanes to give the title compound (98 mg, 58%). MS(ES)+ m/e 321 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592342B2
Source datasetuspto-grants-2009_09
ORD IDord-e2f2bf9bb78249848843f1db36264fb6
Source noteuspto-grants-2009_09