Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 5H,6H,7H,8H-imidazo(1,5-c)pyrimidin-5-one | HCID 1487518 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86616231 | HCID 86616231 | — |
Reaction Steps
A suspension of 7,8-dihydroimidazo[1,5-c]pyrimidin-5(6H)-one, obtained in step I as describe above (500 mg; 3.65 mmol; 1 eq), and bromoethane (816 μl; 10.94 mmol; 3 eq) in DMF (7 ml) is divided in two equals fractions and heated under microwave irradiation at 180° C. for 20 min. The reaction mixtures are combined and acetonitrile (15 ml) is added. The resulting precipitate is filtered, washed with acetonitrile and dried under vacuum, affording the title compound that is used in the next step without further purification (118.3 mg; 13%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07799814B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-1f01aab1ff454ea1a442dcffa9b70849 |
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| Source note | uspto-grants-2010_09 |
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