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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378014Generated: October 30, 2026

Water → HCID 53807155, compound

https://huagongshe.com/reaction/1378014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 54277046HCID 54277046—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 53807155HCID 5380715590.4%

Reaction Steps

6.31 g (21 mmol) of (S)-7-fluoro-9-oxo-11,12,13,13a-tetrahydro-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxamide were suspended in 20 ml of dioxan and 3.6 ml of pyridine and treated dropwise at 5° to 10° with 3.3 ml of trifluoroacetic anhydride. The reaction mixture was stirred at room temperature overnight and poured into 150 ml of water. The suspension obtained was filtered and the crystals were dried. There were obtained 5.36 g (90%) of (S)-7-fluoro-9-oxo-11,12,13,13a-tetrahydro-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carbonitrile of m.p. 254°-256°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665718
Source datasetuspto-grants-1997_09
ORD IDord-63460653439e43b7860c2c32627d105c
Source noteuspto-grants-1997_09