HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569068Generated: October 30, 2026
Acetic Anhydride → HCID 20148569, compound
https://huagongshe.com/reaction/569068
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 54386855 | HCID 54386855 | — |
| Product | HCID 20148569 | HCID 20148569 | 33% |
Reaction Steps
A suspension of N,N-dimethyl-N'-(4-oxido-thieno[3,2-b]pyridine-2-sulfonyl)formamidine (6.23 g, 22.6 mmol) in acetic anhydride (70 ml), under a nitrogen atmosphere, was heated at 140° C. for 20-22 hours to give a dark solution. The excess acetic anhydride was removed on a rotary evaporator and 6 N HCl (90 ml) was added to the residue and it was warmed at 80° C. for four hours. This reaction mixture was cooled and ice was added as product began to precipitate. Upon standing several crops were collected by filtration. The combined crude product (2.2 g) was dissolved in a large volume of boiling water, filtered and allowed to cool. Pure product was obtained (1.72 g, 33% yield). This material was recrystallized by dissolution in a minimum volume of hot dimethylsulfoxide. This solution was treated with charcoal, filtered, and diluted with ethanol as product crystallized (1.3 g), m.p. >300° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04731368 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-dcc7984c6b2a483ab6824a560d76b438 |
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| Source note | uspto-grants-1988_03 |
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