HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787820Generated: October 31, 2026
N-bromobutanimide → 7-bromo-9-pentyl-3-[3-(3-phenyl-1,2,4-oxadiazol-5-yl)propyl]-6,9-dihydro-5H-[1,2,4]triazolo[4,3-a]purin-5-one
https://huagongshe.com/reaction/1787820
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 9-pentyl-3-[3-(3-phenyl-1,2,4-oxadiazol-5-yl)propyl]-6,9-dihydro-5H-[1,2,4]triazolo[4,3-a]purin-5-one | HCID 57600320 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-bromo-9-pentyl-3-[3-(3-phenyl-1,2,4-oxadiazol-5-yl)propyl]-6,9-dihydro-5H-[1,2,4]triazolo[4,3-a]purin-5-one | HCID 57600176 | 21% |
Reaction Steps
To the solution of 9-pentyl-3-[3-(3-phenyl-1,2,4-oxadiazol-5-yl)propyl]-6,9-dihydro-5H-[1,2,4]triazolo[4,3-a]purin-5-one (0.50 g, 1.16 mmole) in THF (125 ml) at room temperature was added N-bromosuccinimide (0.309 g, 1.73 mmole). The mixture was stirred at 70° C. for 1 h. The mixture was concentrated and purified by preparative LCMS to yield the desired product (122 mg, 21% yield). LCMS calculated for C22H24BrN8O2 (M+H): 511.1; found: 511.0.
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-118a8b47000742aebe0f51e7ea0e8e80 |
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| Source note | uspto-grants-2009_03 |
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