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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluorophenylboronic acidHCID 2734354—
Reactant5-Chloro-1H-pyrrolo(3,2-b)pyridineHCID 12384237—
CatalystHCID 178478230HCID 178478230—
Product5-(2-fluorophenyl)-1H-pyrrolo[3,2-b]pyridineHCID 6795996496%

Reaction Conditions

Temperature120 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090593B2
Source datasetuspto-grants-2015_07
ORD IDord-b366e8fc1c1945ba93327ddc84ee759b
Source noteuspto-grants-2015_07