HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-butyl 4-aminophenethylcarbamate → HCID 21876379, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-butyl 4-aminophenethylcarbamate | HCID 382207 | — |
| Reactant | 2,4-Dichloro-6-methyl-3-nitropyridine | HCID 2784819 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Product | HCID 21876379 | HCID 21876379 | 16% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07148234B2 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-1ea2eea511494c8e9f88cc0c7e0343d1 |
| Source note | uspto-grants-2006_12 |