HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → N-cyclopropyl-4'-{5-[(cyclopropylamino)methyl]-1,3,4-oxadiazol-2-yl}-5-fluoro-6-methyl-1,1'-biphenyl-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 4'-[5-(chloromethyl)-1,3,4-oxadiazol-2-yl]-N-cyclopropyl-5-fluoro-6-methyl-1,1'-biphenyl-3-carboxamide | HCID 69314917 | — |
| Solvent | Cyclopropylamine | HCID 69828 | — |
| Product | N-cyclopropyl-4'-{5-[(cyclopropylamino)methyl]-1,3,4-oxadiazol-2-yl}-5-fluoro-6-methyl-1,1'-biphenyl-3-carboxamide | HCID 9978666 | — |
Reaction Steps
4′-[5-(Chloromethyl)-1,3,4-oxadiazol-2-yl]-N-cyclopropyl-5-fluoro-6-methyl-1,1′-biphenyl-3-carboxamide (Intermediate 34) (50 mg) and potassium iodide (22 mg) were stirred in cyclopropylamine (2 ml) for 48 hours. The reaction was absorbed onto silica and purified by chromatography on a biotage column (silica, 9 g), eluting with DCM/methanol (99:1). The product fractions were reduced to dryness under vacuum to give N-cyclopropyl-4′-{5-[(cyclopropylamino)methyl]-1,3,4-oxadiazol-2-yl}-5-fluoro-6-methyl-1,1′-biphenyl-3-carboxamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07425555B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-4cbeb6e1246742cdbcdba57395bf4873 |
| Source note | uspto-grants-2008_09 |