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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378244Generated: November 1, 2026

Trifluoroacetic anhydride → HCID 54313191, compound

https://huagongshe.com/reaction/1378244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 54419029HCID 54419029—
SolventPyridineHCID 1049—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 54313191HCID 5431319180.7%

Reaction Steps

4.44 ml (31.9 mmol) of trifluoroacetic anhydride were added dropwise at 5°-8° to a suspension of 8.98 g (31.1 mmol) of (S)-10,11,12,12a-tetrahydro-8-oxo-8H-imidazo[5,1-c]pyrrolo[1,2-a]thieno[3,2-e][1,4]diazepine-1-carboxamide in 50 ml of dioxan and 5.4 ml of pyridine. The beige solution obtained was stirred at 50° for 2.5 hours and subsequently poured into 220 ml of ice-water. The resulting precipitate was filtered off. After drying at 70°/10 Torr there were obtained 6.78 g (80%) of (S)-10,11,12,12a-tetrahydro-8-oxo-8H-imidazo[5,1-c]pyrrolo[1,2-a]thieno[3,2-e][1,4]diazepine-1-carbonitrile as a white powder of m.p. 249°-251°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665718
Source datasetuspto-grants-1997_09
ORD IDord-e8264862a3ae41bb900b899e70c41219
Source noteuspto-grants-1997_09