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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240474Generated: October 26, 2026

4-[(4-nitro-1H-indol-1-yl)methyl]-1-(t-butyloxycarbonyl)-1H-pyrrolo[2,3-b]pyridine → 4-[(4-amino-1H-indol-1-yl)methyl]-1-(t-butyloxycarbonyl)-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/240474

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[(4-nitro-1H-indol-1-yl)methyl]-1-(t-butyloxycarbonyl)-1H-pyrrolo[2,3-b]pyridineHCID 68748411—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
Product4-[(4-amino-1H-indol-1-yl)methyl]-1-(t-butyloxycarbonyl)-1H-pyrrolo[2,3-b]pyridineHCID 6874900795.5%

Reaction Steps

In a round-bottom flask was added 4-[(4-nitro-1H-indol-1-yl)methyl]-1-(t-butyloxycarbonyl)-1H-pyrrolo[2,3-b]pyridine (500 mg, 1.3 mmol), Palladium on carbon (50 mg, 10%), and THF (30 mL). The mixture was stirred under a hydrogen atmosphere for 2 h, then filtered, concentrated to afford 4-[(4-amino-1H-indol-1-yl)methyl]-1-(t-butyloxycarbonyl)-1H-pyrrolo[2,3-b]pyridine (450 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648086B2
Source datasetuspto-grants-2014_02
ORD IDord-acc086089f984604bbb8543e8607f3a4
Source noteuspto-grants-2014_02