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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454669Generated: November 1, 2026

Tert-butyl 4-aminophenethylcarbamate → HCID 21876379, compound

https://huagongshe.com/reaction/1454669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-aminophenethylcarbamateHCID 382207—
Reactant2,4-Dichloro-6-methyl-3-nitropyridineHCID 2784819—
SolventDiisopropylethylamineHCID 81531—
ProductHCID 21876379HCID 2187637916%

Reaction Steps

A mixture of 2,4-dichloro-6-methyl-3-nitro-pyridine (Chorvat, Robert J. et al., J. Med. Chem., 1999, 42, 833., 7.5 g, 36.2 mmol), [2-(4-amino-phenyl)-ethyl]-carbamic acid tert-butyl ester (Stark, Peter A. et al., J. Med. Chem., 1992, 35, 4264., 1.14 g, 4.83 mmol) in N,N-diisopropylethylamine (50 ml) was heated at reflux temperature for 16 h. After cooling, the mixture was concentrated. The residue was diluted with dichloromethane (200 ml) and washed with saturated aqueous NaHCO3 solution (50 ml×2). The organic layer was dried (MgSO4), and concentrated. Purification by flash column chromatography eluting with hexane/ethyl acetate (1:1) to afford 310 mg (16%) of the title compound as orange solids.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07479564B2
Source datasetuspto-grants-2009_01
ORD IDord-f3d6aa316eff45108e67ed94a147e5de
Source noteuspto-grants-2009_01