Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 67974411 | HCID 67974411 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67973849 | HCID 67973849 | — |
Reaction Steps
5-(5-fluoropyridin-2-yl)-2-(phenoxymethyl)-6,7-dihydropyrazolo[1,5-a]pyrazin-4(5H)-one (100 mg, 0.296 mmol) was dissolved in DCM (2 mL), cooled to 0° C. and treated with 1M BBr3 in DCM (1.18 mmol, 1.18 mL). The reaction was allowed to warm to room temperature and stirred for 4 h. The reaction was diluted with DCM (5 mL) and then washed sequentially with 1M HCl (2 mL), saturated aq. NaHCO3 (2 mL) and 1N NaOH (2 ml). The organic layer was dried over Na2SO4, filtered and concentrated under vacuum to give A (82 mg, 85%) as an oil: LC-MS (215 nm)>98%, 324.8 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592422B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-061af7ffccfc4ec8937641cfd2252e3f |
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| Source note | uspto-grants-2013_11 |
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