Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propylene Oxide | HCID 6378 | — |
| Reactant | HCID 22185184 | HCID 22185184 | — |
| Reactant | HCID 69588867 | HCID 69588867 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10094737 | HCID 10094737 | 26% |
Reaction Steps
To a solution of 1-methyl-3-naphthalen-2-yl-6-pyrrolidin-3-yl-1H-[4,4′]bipyridinyl-2-one (prepared following the same method as described for 1′-methyl-5′-naphthalen-2-yl-1,2,3,4,5,6-hexahydro-1′H-[4,2′;4′,4″]terpyridin-6′-one, Scheme 12) (0.5 g, 1.3 mmol) in dry DMF (5 mL) was added 2-methyl-oxirane (2.6 mmol, 150 mg) and then heated at 80° C. for 5 h. After cooling down to RT the solvent was removed under vacuum and the residue was purified by flash chromatography (2%, 2M methanol ammonia in DCM) to obtain the title compound (150 mg, 26%) as a yellow solid. MS (ES+): 440 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07026326B2 |
|---|
| Source dataset | uspto-grants-2006_04 |
|---|
| ORD ID | ord-b478759b3042425e862c1f112af94da6 |
|---|
| Source note | uspto-grants-2006_04 |
|---|