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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378126Generated: November 2, 2026

Trifluoroacetic anhydride → HCID 22914601, compound

https://huagongshe.com/reaction/1378126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 22914318HCID 22914318—
SolventPyridineHCID 1049—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 22914601HCID 2291460191%

Reaction Steps

8.7 ml (62.9 mmol) of trifluoroacetic anhydride were added dropwise at 5°-8° to a suspension of 15 g (57.2 mmol) of 5-methyl-4-oxo-5,6-dihydro-4H-imidazo[1,5-a]thieno[3,2-f][1,4]diazepine-7-carboxamide in 80 ml of dioxan and 20 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 12.70 g (91%) of 5-methyl-4-oxo-5,6-dihydro-4H-imidazo[1,5-a]thieno[3,2-f][1,4]diazepine-7-carbonitrile as a white powder of m.p. 197°-200°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665718
Source datasetuspto-grants-1997_09
ORD IDord-125c9b6e30244d319566bd59d9a8b1a7
Source noteuspto-grants-1997_09