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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1964459Generated: October 30, 2026

2-tert-butyl-1-(2-hydroxyethyl)-5-nitro-1H-indole-4-carbonitrile → 5-amino-2-tert-butyl-1-(2-hydroxyethyl)-1H-indole-4-carbonitrile

https://huagongshe.com/reaction/1964459

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-tert-butyl-1-(2-hydroxyethyl)-5-nitro-1H-indole-4-carbonitrileHCID 58183244—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product5-amino-2-tert-butyl-1-(2-hydroxyethyl)-1H-indole-4-carbonitrileHCID 5818322293%

Reaction Steps

To a solution of 2-tert-butyl-1-(2-hydroxyethyl)-5-nitro-1H-indole-4- carbonitrile (180 mg, 0.63 mmol) in ethanol (6 mL) under N2 atmosphere was added Pd—C (5% wt, 18 mg). The reaction was flushed with N2 (g) and then with H2 (g) and stirred under H2 (atm) at room temperature for 1.5 hours. The reaction was filtered over Celite and concentrated to yield the product (150 mg, 93%). ESI-MS m/z calc. 257.2, found 258.5 (M+1)+. Retention time 1.26 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415387B2
Source datasetuspto-grants-2013_04
ORD IDord-f9fa86a51f184626befb979bcc6bd385
Source noteuspto-grants-2013_04