HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13400Generated: October 29, 2026
Dimethylformamide → t-Butyl 2-(4-amino-2-((2'-fluorobiphenyl-4-yl)oxy)-5-nitrophenyl)pyrrolidine-1-carboxylate
https://huagongshe.com/reaction/13400
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(2-Fluorophenyl)phenol | HCID 345419 | — |
| Reactant | t-Butyl 2-(4-amino-2-fluoro-5-nitrophenyl)pyrrolidine-1-carboxylate | HCID 23145290 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | t-Butyl 2-(4-amino-2-((2'-fluorobiphenyl-4-yl)oxy)-5-nitrophenyl)pyrrolidine-1-carboxylate | HCID 23145747 | — |
Reaction Steps
200 mg of 2′-fluorobiphenyl-4-ol and 184 mg of potassium carbonate were added to an N,N-dimethylformamide (3 ml) solution of 288 mg of t-butyl 2-(4-amino-2-fluoro-5-nitrophenyl)pyrrolidine-1-carboxylate, and the reaction liquid was stirred overnight at 80° C. The reaction liquid was diluted with ethyl acetate, washed with water and saturated saline in order, and dried with anhydrous magnesium sulfate. The solvent was evaporated away, and the resulting residue was purified through silica gel column chromatography (developing solvent: hexane/ethyl acetate=5/1) to obtain the entitled compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07728025B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-88334f19c84844df8c80809518875144 |
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| Source note | uspto-grants-2010_06 |
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