HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754751Generated: October 30, 2026
Trifluoroacetic acid → HCID 57619272, compound
https://huagongshe.com/reaction/1754751
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | HCID 57619414 | HCID 57619414 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 57619272 | HCID 57619272 | 105% |
Reaction Steps
To 5-[(1-benzenesulfonyl-5-methoxy-1H-pyrrolo[2, 3-1)]pyridin-3-yl)-hydroxy-methyl]-6-fluoro-pyridin-2-yl-(6-trifluoromethyl-pyridin-3-ylmethyl)-carbamic acid tert-butyl ester (576, 0.100 g, 0.15 mmol) in acetonitrile (12.6 mL) were added triethylsilane (0.34 mL, 2.10 mmol) and trifluoroacetic acid (0.17 mL, 2.20 mmol). The reaction was heated to 80° C. for 2 hours. The reaction was poured into aqueous potassium carbonate, and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated to give the crude compound (577, 90 mg, 100%) that was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09169250B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-4e74265363584784b16dcbb4e5aa70a7 |
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| Source note | uspto-grants-2015_10 |
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