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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205980Generated: November 1, 2026

Trifluoroacetic anhydride → HCID 117987805, compound

https://huagongshe.com/reaction/2205980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 117988213HCID 117988213—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
ProductHCID 117987805HCID 11798780574.9%

Reaction Steps

To a solution of 4-(4-oxo-1-(pentan-3-yl)-4,5-dihydro-1H-pyrrolo[3,2-c]pyridin-3-yl)thiophene-2-carboxamide (13.0 mg) obtained in Example 8 in DMA (2 mL) was slowly added dropwise trifluoroacetic anhydride (8.36 μL) under nitrogen atmosphere at 0° C., and the mixture was allowed to be warmed to room temperature, and stirred overnight at room temperature. The reaction mixture was diluted with water, and the mixture was extracted three times with ethyl acetate. The combined organic layers were washed with saturated brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (basic silica gel, ethyl acetate) to give the title compound (9.2 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371320B2
Source datasetuspto-grants-2016_06
ORD IDord-c0b634858d62429fae797a12ccbbae04
Source noteuspto-grants-2016_06