Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-Norbornyl bromide | HCID 98232 | — |
| Reactant | HCID 57418557 | HCID 57418557 | — |
| Reactant | HCID 57503084 | HCID 57503084 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57503084 | HCID 57503084 | 9% |
| Product | HCID 57503085 | HCID 57503085 | 30% |
Reaction Steps
1-Bicyclo[2.2.1]hept-2-yl-5-chloro-3-p-tolyl-13-dihydro-imidazo[4,5-b]pyridine-2-one (38) and 2-(Bicyclo[2.2.1]hept-2-yloxy)-5-chloro-3-p-tolyl-3H-imidazo[4,5-b]pyridine (39). A mixture of 5-Chloro-3-p-tolyl-1,3-dihydro-imidazo[4,5-b]pyridine-2-one (52 mg, 0.2 mmol), exo-2-bromonorbornane (103 μL, 0.8 mmol) and Cs2CO3 (195 mg, 0.6 mmol) in 1.5 mL DMF was heated in microwave at 200° C. for 20 min. After filtration, the filtrate was diluted with EtOAc, washed with water. The organic phase was concentrated, the residue was dissolved in a minimum amount of DCM, and subjected to silica gel column purification to give 21.2 mg (yield: 30%) 1-Bicyclo[2.2.1]hept-2-yl-5-chloro-3-p-tolyl-1,3-dihydro-imidazo[4,5-b]pyridine-2-one (Rf=0.60 in DCM) and 6.2 mg (yield: 9%) 2-(Bicyclo[2.2.1]hept-2-yloxy)-5-chloro-3-p-tolyl-3H-imidazo[4,5-b]pyridine (Rf=0.49 in DCM). Calculated mass=353. Observed mass=354.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07749999B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-e25e05e4ae064bf99f7448f72b9753ff |
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| Source note | uspto-grants-2010_07 |
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