HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734961Generated: November 4, 2026
Acetic Anhydride → HCID 57843254, compound
https://huagongshe.com/reaction/734961
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | HCID 68506108 | HCID 68506108 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 57843254 | HCID 57843254 | 58.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07592342B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-e2f2bf9bb78249848843f1db36264fb6 |
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| Source note | uspto-grants-2009_09 |
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