HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-allyl-N-(3-ethylphenyl)-1H-pyrrole-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Ethylaniline | HCID 11475 | — |
| Reactant | Bis(2-oxo-3-oxazolidinyl)phosphinic chloride | HCID 152842 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | 1-(prop-2-en-1-yl)-1H-pyrrole-2-carboxylic acid | HCID 45082008 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-allyl-N-(3-ethylphenyl)-1H-pyrrole-2-carboxamide | HCID 22928687 | 50.3% |
Reaction Steps
A mixture of 1-allyl-1H-pyrrole-2-caboxylic acid (270 mg, 1.79 mmol), m-ethylaniline (0.43 g, 2.48 mmol), BOP-Cl (500 mg, 1.96 mmol) and triethylamine (210 mg, 2.08 mmol) in dichloromethane (3 ml) was stirred for 2 hours at room temperature. To the reaction mixture was added an aqueous 5% potassium hydrogensulfate solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water, an aqueous saturated sodium hydrogencarbonate solution and an aqueous saturated sodium chloride solution, and dried over magnesium sulfate. The solvent was removed and the residue was purified with silica gel chromatography (hexane:ethyl acetate=5:1→3:1) to give the subject compound (229 mg, 50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07220773B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-66308b2ef61e4ea69cc21d7056b756be |
| Source note | uspto-grants-2007_05 |