HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → {2-[2-(Dimethylamino)-3-nitropyrrolyl]ethyl}[(6-chloro(3-pyridyl))methyl][(4-chlorophenyl)methyl]amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N,N-Dimethyl-3-nitro-1H-pyrrol-2-amine | HCID 45121913 | — |
| Reactant | (6-Chloro(3-pyridyl)methyl](2-chloroethyl)[(4-chlorophenyl)methyl]amine | HCID 86624870 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | {2-[2-(Dimethylamino)-3-nitropyrrolyl]ethyl}[(6-chloro(3-pyridyl))methyl][(4-chlorophenyl)methyl]amine | HCID 86624871 | — |
Reaction Steps
This compound was prepared in a manner analogous to that set forth in Step G of Example 1, using 0.47 gram (0.0014 mole) of [(6-chloro(3-pyridyl)methyl](2-chloroethyl)[(4-chlorophenyl)methyl]amine (prepared in Steps A and B of the present Example), 0.2 gram (0.0013 mole) of dimethyl(3-nitropyrrol-2-yl)amine and 0.45 gram (0.0032 mole) of potassium carbonate in 20 mL of DMF. The crude product was purified with column chromatography on silica gel. Elution was accomplished using 50% hexane in diethyl as an eluant. The appropriate fractions were combined and concentrated under reduced pressure, yielding 0.05 gram of Compound 214. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07943642B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-e6894f8dcb064c0eaed8eda8d7f4875a |
| Source note | uspto-grants-2011_05 |