HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cesium carbonate → N-[4-(3-fluoro-4-nitro-anilino)-2-pyridyl]cyclopropanecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Cyclopropanecarboxamide | HCID 80376 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | 2-chloro-N-(3-fluoro-4-nitro-phenyl)-N-methyl-pyridin-4-amine | HCID 90020477 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-[4-(3-fluoro-4-nitro-anilino)-2-pyridyl]cyclopropanecarboxamide | HCID 90020584 | 74.4% |
Reaction Steps
Add 2-chloro-N-(3-fluoro-4-nitro-phenyl)-N-methyl-pyridin-4-amine (190 mg, 0.68 mmol), cyclopropanecarboxamide (85 mg, 2.03 mmol), Cs2CO3 (440 mg, 1.35 mmol), (±)-2,2′-bis(diphenylphosphino)-1,1′-binaphthalene (BINAP, 43 mg, 0.05 mmol) and tris(dibenzylideneacetone)dipalladium [Pd2(dba)3, 42 mg, 0.07 mmol] in 1,4-dioxane (6 mL) under N2. Heat the reaction at 125° C. for 16 hrs. TLC (EtOAc:PE=2:1) shows the reaction is complete. Cool to room temperature, filter, and concentrate the filtrate under reduced pressure to give the crude product. Purification by chromatography (silica gel, EtOAc:PE=2:1) affords the target compound (160 mg, 71.7%). MS: (M+1): 331.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09359338B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-d629941ff8bf4df5b9f6f0419ee2d4f3 |
| Source note | uspto-grants-2016_06 |