HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509974Generated: November 2, 2026
Trifluoroacetic acid → HCID 67200202, compound
https://huagongshe.com/reaction/509974
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | HCID 67201062 | HCID 67201062 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 67200202 | HCID 67200202 | — |
Reaction Steps
To {5-[(1-benzenesulfonyl-5-methoxy-1H-pyrrolo[2,3-b]pyridin-3-yl)-hydroxy-methyl]-pyrimidin-2-yl}-(5-fluoro-2-methoxy-pyridin-3-ylmethyl)-carbamic acid tert-butyl ester (124, 1 equivalent) in 10.0 mL of acetonitrile, triethylsilane (15.6 equivalents) and trifluoroacetic acid (16.9 equivalents) are added. The reaction is heated at 80° C. for 2 hours, then poured into aqueous potassium carbonate and extracted with ethyl acetate. The organic layer is dried over sodium sulfate, filtered and the filtrate concentrated under vacuum to provide the desired compound, which is used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096593B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-8581bd83d614468f8d989709420824f9 |
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| Source note | uspto-grants-2015_08 |
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