HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811909Generated: October 26, 2026
2-Chloroquinoline-3-boronic acid → 2-Chloro-3-(2-methyl-9-(tetrahydro-2H-pyran-2-YL)-9H-purin-6-YL)quinoline
https://huagongshe.com/reaction/1811909
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chloroquinoline-3-boronic acid | HCID 4198643 | — |
| Reactant | 6-chloro-2-methyl-9-(tetrahydro-2H-pyran-2-yl)-9H-purine | HCID 59548268 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Chloro-3-(2-methyl-9-(tetrahydro-2H-pyran-2-YL)-9H-purin-6-YL)quinoline | HCID 86647052 | — |
Reaction Steps
A mixture of 6-chloro-2-methyl-9-(tetrahydro-2H-pyran-2-yl)-9H-purine (0.55 g, 2.18 mmol), 2-chloroquinolin-3-ylboronic acid (0.90 g, 4.35 mmol, Aldrich, St. Louis, Mo.) and tetrakis(triphenylphosphine)palladium(0) (0.13 g, 0.11 mmol, Strem Chemicals, Inc., Newburyport, Mass.) in dioxane (3 mL) and water (1 mL) was sealed and purged with argon for several minutes. The reaction mixture was stirred at 90° C. for 6 h and then allowed to cool to room temperature. The organic phase was taken and the solvents removed under vacuum. Purification of the crude reaction mixture by silica gel chromatography (0 to 3% MeOH/CH2Cl2) provided the title compound as an orange solid. m/z (ESI, +ve ion) 380 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362241B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-e6bf2c1d28ed41ac871beb8d9c2a5375 |
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| Source note | uspto-grants-2013_01 |
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