HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600429Generated: October 29, 2026
1-Butanol → 2-(6-fluoro-1H-benzo[d]imidazol-1-yl)-9-((R)-8-fluorochroman-4-yl)-6-phenyl-7H-purin-8(9H)-one
https://huagongshe.com/reaction/600429
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 6-chloro-2-(6-fluoro-1H-benzo[d]imidazol-1-yl)-9-((R)-8-fluorochroman-4-yl)-7H-purin-8(9H)-one | HCID 57612698 | — |
| Product | 2-(6-fluoro-1H-benzo[d]imidazol-1-yl)-9-((R)-8-fluorochroman-4-yl)-6-phenyl-7H-purin-8(9H)-one | HCID 57612684 | — |
Reaction Steps
General procedure for displacement reactions of 6-chloropurinones with aliphatic amines. To 10 mg (0.022 mmol) of 6-chloro-2-(6-fluoro-1H-benzo[d]imidazol-1-yl)-9-((R)-8-fluorochroman-4-yl)-7H-purin-8(9H)-one was added 0.6 mL of 1-butanol, followed by an aliphatic amine (0.1 mL), and the reaction mixture was stirred at 110° C. for 1-2 h (HPLC monitoring). Upon completion of the reaction, the mixture was left to cool to room temperature, was diluted with acetonitrile and filtered through a Nylon 0.45 μm filter. Preparative HPLC purification afforded, after solvent evaporation and drying, the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07902187B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-a2cce3db24864e4e8dfe0a72f08362c5 |
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| Source note | uspto-grants-2011_03 |
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