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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1711035Generated: October 31, 2026

7-(2-fluoro-4-nitrophenoxy)-1H-pyrrolo[2,3-c]pyridine → 4-(1H-Pyrrolo[2,3-c]pyridin-7-yloxy)-3-fluorobenzenamine

https://huagongshe.com/reaction/1711035

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-(2-fluoro-4-nitrophenoxy)-1H-pyrrolo[2,3-c]pyridineHCID 59424641—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
Product4-(1H-Pyrrolo[2,3-c]pyridin-7-yloxy)-3-fluorobenzenamineHCID 5942462999.4%

Reaction Steps

To a solution of 260 (100 mg, 0.36 mmol) in AcOH (4 mL) at 90° C., was added iron powder (102 mg, 2.1 mmol). The reaction mixture was vigorously stirred for 10 min, cooled, filtered through a Celite pad and concentrated. The residue was purified by flash column chromatography, eluent EtOAc/hexane (1:1), to afford title compound 261 (87 mg, 99% yield) as an off-white solid. MS (m/z): 244.1 (M+H) (found).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790729B2
Source datasetuspto-grants-2010_09
ORD IDord-f27097951d65493a9321f93e0585f95f
Source noteuspto-grants-2010_09