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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218245Generated: October 26, 2026

2-Amino-6-(2-{[tert-butyl(dimethyl)silyl]oxy}phenyl)-4-(3-nitrophenyl)nicotinonitrile → 2-Amino-4-(3-aminophenyl)-6-(2-{[tert-butyl(dimethyl)silyl]oxy}phenyl)nicotinonitrile

https://huagongshe.com/reaction/2218245

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-6-(2-{[tert-butyl(dimethyl)silyl]oxy}phenyl)-4-(3-nitrophenyl)nicotinonitrileHCID 68953563—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product2-Amino-4-(3-aminophenyl)-6-(2-{[tert-butyl(dimethyl)silyl]oxy}phenyl)nicotinonitrileHCID 59769674—

Reaction Steps

A mixture of 2-amino-6-(2-{[tert-butyl(dimethyl)-silyl]oxy}phenyl)-4-(3-nitrophenyl)nicotinonitrile (3.2 g, 7.2 mmol), 10% Pd—C (0.25 g) and ethyl acetate (1 L) was stirred at room temperature for 12 hrs. under a hydrogen atmosphere (2.5 atm). The reaction mixture was filtered on Celite Pad and the filtration was concentrated under reduced pressure to give starting compound 2, which was used for the next step without further purification (2.6 g, yield 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07410986B2
Source datasetuspto-grants-2008_08
ORD IDord-1a403d450baf4afab16480e576beb463
Source noteuspto-grants-2008_08