HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243573Generated: October 31, 2026
Trifluoroacetic acid → HCID 11635079, compound
https://huagongshe.com/reaction/2243573
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 58608123 | HCID 58608123 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11635079 | HCID 11635079 | — |
Reaction Steps
A solution of 4-(2-{2-[4-(2-morpholin-4-yl-ethoxy)-phenyl]-3-phenyl-furo[2,3-b]pyridin-4-ylamino}-ethyl)-piperazine-1-carboxylic acid tert-butyl ester 10d (0.062 g, 0.099 mmol) in dichloromethane (1.0 mL) was cooled to 0° C. Trifluoroacetic acid (0.5 mL) was added and the solution stirred under a nitrogen atmosphere at 0° C. for 15 min and then at room temperature for 2.5 h. The reaction mixture was concentrated and the residue was partitioned between ethyl acetate and saturated aqueous sodium bicarbonate solution. The organic phase was separated and washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, filtered and concentrated to afford 2-(4-((2-(4-morpholinyl)ethyl)oxy)phenyl)-3-phenyl-N-(2-(1-piperazinyl)ethyl)furo[2,3-b]pyridin-4-amine 10e as an off-white solid. MS (MH+) 528.3; Calculated 527 for C31H37N5O3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07674907B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-9f7ab69883954c83bdf603d9c0bbc8e2 |
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| Source note | uspto-grants-2010_03 |
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