HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253480Generated: October 31, 2026
Trifluoroacetic acid → HCID 178488773, compound
https://huagongshe.com/reaction/253480
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | HCID 178492500 | HCID 178492500 | — |
| Reactant | HCID 178492554 | HCID 178492554 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178488773 | HCID 178488773 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07872018B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-2aac62a3c0d044a3be998d8d48d186d8 |
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| Source note | uspto-grants-2011_01 |
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