HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024309Generated: October 29, 2026
Trifluoroacetic acid → HCID 57619310, compound
https://huagongshe.com/reaction/1024309
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 57619315 | HCID 57619315 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57619310 | HCID 57619310 | 29% |
Reaction Steps
To the solution of crude [5-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-thiazol-2-yl]-(4-fluoro-benzyl)-carbamic acid tert-butyl ester (628, 0.186 mmol theory) in dichloromethane (5 mL) at room temperature was added trifluoroacetic acid (1 mL) and the reaction was allowed to stir overnight. The solvent was removed in vacuo and the residue taken up in ethyl acetate and then washed with saturated aqueous potassium carbonate making sure basicity was reached. The layers were separated and the aqueous layer was back-extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate and evaporated in vacuo to give the crude product which was purified by silica gel chromatography (0-10% methanol/ethyl acetate). The solvent was removed in vacuo and the material was triturated with dichloromethane to give the desired compound as an off-white solid (20 mg, 29% over 2 steps) consistent with compound structure by 1H-NMR and
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722702B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-994cb06628da43ceb04d20c125138c8e |
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| Source note | uspto-grants-2014_05 |
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