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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173118Generated: November 2, 2026

Tetrahydrofuran → 4-Bromo-7-isoquinolinamine

https://huagongshe.com/reaction/1173118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 22674041HCID 22674041—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-Bromo-7-isoquinolinamineHCID 2267405756.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

66 mg (0.26 mmol) of 7-nitro-4-bromoisoquinoline was dissolved in 1 ml of ethanol, 2 ml of tetrahydrofuran and 1 ml of water. To the mixture were added 70 mg of an iron powder and 140 mg of ammonium chloride, followed by heating at 50° C. for 3 hours. A 1N aqueous sodium hydroxide was added to the reaction solution, and the mixture was extracted with chloroform. The organic layer was dried over magnesium sulfate and concentrated. The resulting residue was crystallized from isopropyl ether, to give 33 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834049B2
Source datasetuspto-grants-2010_11
ORD IDord-55d99ed0bf664372b1486baab47e5983
Source noteuspto-grants-2010_11