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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858476Generated: October 30, 2026

Tert-butyl 4-aminophenethylcarbamate → HCID 21876379, compound

https://huagongshe.com/reaction/858476

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 numberUS07148234B2
Source datasetuspto-grants-2006_12
ORD IDord-1ea2eea511494c8e9f88cc0c7e0343d1
Source noteuspto-grants-2006_12