HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418308Generated: November 1, 2026
Bromocyclopentane → HCID 131721174, compound
https://huagongshe.com/reaction/1418308
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromocyclopentane | HCID 8728 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 131721169 | HCID 131721169 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 131721174 | HCID 131721174 | 67.4% |
Reaction Steps
An acetonitrile (10 mL) solution of 2-(2-chloro-4-methyl-5-hydroxyphenyl)-5,6-dihydroimidazo [1,5-a] pyridine-1,3[2H, 7H]-dione (0.34 g, 1.11 mmol), cyclopentylbromide (0.13 mL, 1.22 mmol) and potassium carbonate (0.15 g, 1.11 mmol) was stirred for 4 hours under reflux. A saturated ammonium chloride solution (20 mL) was added to the resulting mixture and the organic layer was separated. The aqueous layer was extracted with diethyl ether (10 mL×2 times), and the organic layer combined was washed with a saturated sodium chloride solution (40 mL) and dried over anhydrous magnesium sulfate. After removal of magnesium sulfate by filtration, the filtrate was evaporated to give crude product, which was purified by silica gel column (Wakogel C-200, ethyl acetate/hexane=1/2) to obtain a white solid of 2-(2-chloro-5-cyclopentyloxy-4-methylphenyl)-5,6-dihydroimidazo [1,5-a] pyridine-1,3[2H, 7H]-dione (0.27 g, yield:64.3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05883049 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-718ad704c1a74770b985226ff51721fa |
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| Source note | uspto-grants-1999_03 |
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