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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237385Generated: October 30, 2026

5-Bromo-2-methyl-8-nitro-1,2,3,4-tetrahydroisoquinoline → 5-Bromo-2-methyl-1,2,3,4-tetrahydroisoquinolin-8-amine

https://huagongshe.com/reaction/2237385

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2-methyl-8-nitro-1,2,3,4-tetrahydroisoquinolineHCID 10016010—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product5-Bromo-2-methyl-1,2,3,4-tetrahydroisoquinolin-8-amineHCID 9991914—

Reaction Steps

To a solution of N-methyl-5-bromo-8-nitro-1,2,3,4-tetrahydroisoquinoline (III, 4.7 gm, 17.3 mmol) in ethanol (50 ml), Raney Nickel (solution in water, 1.5 g) was added. The reaction mixture was stirred at room temperature overnight under H2. The mixture was filtered through celite and solvent was removed under vacuum to give IV.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718641B2
Source datasetuspto-grants-2010_05
ORD IDord-7c5288c394f14f128e7b45d721e163bd
Source noteuspto-grants-2010_05