HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexanemethylamine → Methyl {4-[(cyclohexylmethyl)amino]-3-nitrophenyl}carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexanemethylamine | HCID 76688 | — |
| Reactant | Methyl (4-fluoro-3-nitrophenyl)carbamate | HCID 3636899 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Methyl {4-[(cyclohexylmethyl)amino]-3-nitrophenyl}carbamate | HCID 57591003 | — |
Reaction Steps
Methyl(4-fluoro-3-nitrophenyl)carbamate (1.00 g, 4.67 mmol) and cyclohexylmethyl amine (0.730 mL, 5.60 mmol) were stirred in EtOH (20 mL) containing TEA (1.0 mL, 7.00 mmol) at 75° C. for 24 h. The solvent was concentrated. The residue was dissolved in EtOAc and washed with 5% KHSO4 aqueous solution, saturated NaHCO3 aqueous solution, brine and dried over anhydrous MgSO4. The crude product was purified by flash chromatography using 4:1/hexanes:EtOAc on silica gel. Yield: 1.05 g (73%); 1H NMR (400 MHz, CHLOROFORM-D) δ 1.04 (m, 2H), 1.25 (m, 3H), 1.69 (m, 2H), 1.77 (m, 2H), 1.83 (m, 1H), 1.86 (m, 1H), 3.14 (m, 2H), 3.78 (s, 3H), 6.46 (m, 1H), 6.84 (d, J=9.37, 1H), 7.63 (m, 1H), 8.05 (d, J=2.54 Hz, 1H), 8.09 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07501447B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-b7cdc726aa8545ffacfb760efffc8f3b |
| Source note | uspto-grants-2009_03 |