HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664585Generated: October 29, 2026
N-bromobutanimide → 7-bromo-9-pentyl-3-[3-(4-phenyl-1H-pyrazol-1-yl)propyl]-6,9-dihydro-5H-[1,2,4]triazolo[4,3-a]purin-5-one
https://huagongshe.com/reaction/1664585
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 9-pentyl-3-[3-(4-phenyl-1H-pyrazol-1-yl)propyl]-6,9-dihydro-5H-[1,2,4]triazolo[4,3-a]purin-5-one | HCID 57600212 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-bromo-9-pentyl-3-[3-(4-phenyl-1H-pyrazol-1-yl)propyl]-6,9-dihydro-5H-[1,2,4]triazolo[4,3-a]purin-5-one | HCID 57600234 | 38.3% |
Reaction Steps
To a solution of 9-pentyl-3-[3-(4-phenyl-1H-pyrazol-1-yl)propyl]-6,9-dihydro-5H-[1,2,4]triazolo[4,3-a]purin-5-one (234 mg, 0.543 mmol) in THF (45 ml) at room temperature was added N-bromosuccinimide (145 mg, 0.814 mmol). After stirring at 70° C. for 1 hour, the reaction mixture was concentrated and then purified by preparative LCMS to give the desired product (106 mg, 38%) as white solid. LCMS calculated for C23H26BrN8O (M+H): 509.1, 511.1. found: 509.0, 511.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08039478B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-c3e502593efe4909ba7a0678e82574fc |
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| Source note | uspto-grants-2011_10 |
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