HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1529342Generated: November 1, 2026
2-Fluorophenylboronic acid → 5-(2-fluorophenyl)-1H-pyrrolo[3,2-b]pyridine
https://huagongshe.com/reaction/1529342
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Fluorophenylboronic acid | HCID 2734354 | — |
| Reactant | 5-Chloro-1H-pyrrolo(3,2-b)pyridine | HCID 12384237 | — |
| Catalyst | HCID 178478230 | HCID 178478230 | — |
| Product | 5-(2-fluorophenyl)-1H-pyrrolo[3,2-b]pyridine | HCID 67959964 | 96% |
Reaction Steps
A mixture of 5-chloro-1H-pyrrolo[3,2-b]pyridine (150 mg, 0.983 mmol, Matrix Scientific), 2-fluorophenylboronic acid (275 mg, 1.966 mmol, Aldrich) and dichloro 1,1′-bis(diphenylphosphino)ferrocene palladium (II) (80 mg, 0.098 mmol, Strem) was capped, degassed and backfilled with argon (3×). Toluene (2 mL), EtOH (2 mL) and Na2CO3, 2.0 M (0.983 mL, 1.966 mmol) were added, and the reaction was heated to 120° C. in a microwave for 45 min. The solution was diluted with EtOAc (50 mL) and washed with brine (50 mL), dried over MgSO4, concentrated in vacuo and purified by silica gel chromatography (eluent: 1-4% MeOH/DCM), affording 5-(2-fluorophenyl)-1H-pyrrolo[3,2-b]pyridine (200 mg, 96%). MS (ESI, pos. ion) m/z: 213.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09090593B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-b366e8fc1c1945ba93327ddc84ee759b |
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| Source note | uspto-grants-2015_07 |
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