HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378030Generated: October 31, 2026
Trifluoroacetic anhydride → HCID 54174090, compound
https://huagongshe.com/reaction/1378030
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | HCID 53747560 | HCID 53747560 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 54174090 | HCID 54174090 | 1,658.3% |
Reaction Steps
5.75 ml (41.3 mmol) of trifluoroacetic anhydride were added dropwise at 5°-8° to a suspension of 11.05 g (40.:2 mmol) of (S)-8-oxo-11,11a-dihydro-8H,10H-azeto[1,2-a]imidazo[5,1-c]thieno[3,2-e][1,4]diazepine-1-carboxamide in 55 ml of dioxan and 7 ml of pyridine. The beige solution obtained was stirred at 50° for 2.5 hours and subsequently poured into 50 ml of ice-water. Extraction with methylene chloride (four times), drying over sodium sulfate, filtration and evaporation yielded a pale brown residue which was chromatographed (silica gel, methylene chloride/methanol 10:1). There were obtained 8.5 g (82%) of (S)-8-oxo-11,11a-dihydro-8H,10H-azeto[1,2-a]imidazo[5,1-c]thieno[3,2-e][1,4]diazepine-1-carbonitrile as a white powder of m.p. 211°-213°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05665718 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-b24cda78172c4e8899494571d1b89bee |
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| Source note | uspto-grants-1997_09 |
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