HuagongsheHuagongshe Chemistry Print Report · For research reference only
t-Butyl 2-(4-amino-2-((2'-fluorobiphenyl-4-yl)oxy)-5-nitrophenyl)pyrrolidine-1-carboxylate → t-Butyl 2-(4,5-diamino-2-((2'-fluorobiphenyl-4-yl)oxy)phenyl)pyrrolidine 1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | t-Butyl 2-(4-amino-2-((2'-fluorobiphenyl-4-yl)oxy)-5-nitrophenyl)pyrrolidine-1-carboxylate | HCID 23145747 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | t-Butyl 2-(4,5-diamino-2-((2'-fluorobiphenyl-4-yl)oxy)phenyl)pyrrolidine 1-carboxylate | HCID 23145792 | — |
Reaction Steps
1 ml of developed Raney nickel was added to a methanol (5 ml) solution of 410 mg of t-butyl 2-(4-amino-2-((2′-fluorobiphenyl-4-yl)oxy)-5-nitrophenyl)pyrrolidine-1-carboxylate, and the reaction liquid was stirred in a hydrogen atmosphere at room temperature for 1 day. The catalyst was removed through filtration through Celite, and the solvent was evaporated away under reduced pressure, and the residue was purified through silica gel column chromatography (developing solvent: hexane/ethyl acetate=1/1) to obtain the entitled compound as a brown oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07728025B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-3a02d6f248624bc2a1e054512125231a |
| Source note | uspto-grants-2010_06 |