HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927518Generated: October 27, 2026
Hydrochloric Acid → 6-(3-Chloro-phenyl)-5-cyclopentyl-pyridine-2-carboxylic acid
https://huagongshe.com/reaction/927518
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (3-Chlorophenyl)boronic acid | HCID 2734323 | — |
| Reactant | 6-Bromo-5-cyclopentyl-pyridine-2-carboxylic acid methyl ester | HCID 86674764 | — |
| Catalyst | HCID 178418807 | HCID 178418807 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-(3-Chloro-phenyl)-5-cyclopentyl-pyridine-2-carboxylic acid | HCID 71087552 | 20.5% |
Reaction Steps
6-Bromo-5-cyclopentyl-pyridine-2-carboxylic acid methyl ester (0.6 g, 2.1 mmol), bis(diphenylphosphino)ferrocene-palladium(II)dichloride methylene chloride complex (CAN 95464-05-4, 90 mg, 0.11 mmol) and potassium carbonate (0.37 g, 2.68 mmol) were added to a solution of 3-chlorophenylboronic acid (CAN 63503-60-6, 0.42 g, 2.69 mmol) in water (20 mL) and DMF (2 mL). The mixture was stirred for 48 h at 100° C. Its pH was adjusted to pH=3 with diluted hydrochloric acid. The mixture was extracted with methylene chloride (3×20 mL). The organic layers were combined, dried over sodium sulfate and concentrated under reduced pressure to give the title compound (130 mg, 20%) which was used in the next step without further purification; MS (EI): m/e=302.0 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09290451B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-f5a7280693d34bc1a0fda956581c009c |
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| Source note | uspto-grants-2016_03 |
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