Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 57600155 | HCID 57600155 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57600276 | HCID 57600276 | 76% |
Reaction Steps
To a mixture of 3-(2-aminoethyl)-9-pentyl-6,9-dihydro-5H-[1,2,4]triazolo[4,3-a]purin-5-one (310 mg, 1.1 mmol) in THF (50 mL), was added N-Bromosuccinimide (0.29 g, 1.6 mmol). The mixture was stirred at 70° C. for 1 hour. The reaction mixture was concentrated. The solid was filtered and washed with EtOAc to yield the desired product (300 mg, 76% yield). LCMS calculated for C13H19BrN7O (M+H): 368.1, 370.1; found: 368.0, 370.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07511050B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-30bcb777201b43de839009bee00a8066 |
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| Source note | uspto-grants-2009_03 |
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