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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253480Generated: October 31, 2026

Trifluoroacetic acid → HCID 178488773, compound

https://huagongshe.com/reaction/253480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
ReactantHCID 178492500HCID 178492500—
ReactantHCID 178492554HCID 178492554—
SolventAcetonitrileHCID 6342—
ProductHCID 178488773HCID 178488773—

Reaction Conditions

Temperature60 °C

Reaction Steps

[4-(5-chloro-1H-benzoimidazol-2-ylmethoxy)-2-fluoro-5-methoxy-phenyl]-(5-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-methanol (228a) and 5-chloro-2-{5-fluoro-2-methoxy-4-[methoxy-(5-methyl-1H-pyrrolo[2,3-b]pyridin-3-yl)-methyl]-phenoxymethyl}-1H-benzoimidazole (228b) were dissolved in acetonitrile. Triethylsilane was added followed by trifluoroacetic acid. The reaction was stirred for one hour at 60° C. The solvent was removed under reduced pressure, Ethyl acetate was added and the organic layer was washed with sodium bicarbonate saturated solution and brine, then dried over anhydrous sodium sulfate and concentrated. Purification with silica gel column chromatography, eluting with a gradient of methanol (2-25%) in dichloromethane, provided the desired compound P-2184. MS (ESI): [M+H+]+=451.0, [M−H+]−=449.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872018B2
Source datasetuspto-grants-2011_01
ORD IDord-2aac62a3c0d044a3be998d8d48d186d8
Source noteuspto-grants-2011_01