HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 4-(2-Tert-butyl-4-nitrothiophene-5-carbonyl)-1-(2-(dimethylamino)ethyl)-3,3-dimethylpiperazin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-(2-(Dimethylamino)ethyl)-3,3-dimethylpiperazin-2-one | HCID 58679203 | — |
| Reactant | 5-Tert-butyl-3-nitrothiophene-2-carboxylic acid | HCID 58679206 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | 4-(2-Tert-butyl-4-nitrothiophene-5-carbonyl)-1-(2-(dimethylamino)ethyl)-3,3-dimethylpiperazin-2-one | HCID 58679224 | 85% |
Reaction Steps
A stirred solution of 5-tert-butyl-3-nitrothiophene-2-carboxylic acid (0.214 g, 0.933 mmol) in 2 ml thionyl chloride was warmed at 45° C. for 1 h and then concentrated under vacuum. The residue was dissolved in 2 ml THF and added to a 3 ml THF solution of 1-(2-(dimethylamino)ethyl)-3,3-dimethylpiperazin-2-one (0.242 g, 1.21 mmol) and DIEA (0.362 g, 2.80 mmol). The resulting mixture was stirred at room temperature for 5 minutes, diluted with ethyl acetate, washed with 1N HCl, water, brine, dried and the solvent eliminated under vacuum to yield 0.300 g, (˜85% purity) of 4-(2-tert-butyl-4-nitrothiophene-5-carbonyl)-1-(2-(dimethylamino)ethyl)-3,3-dimethyl-piperazin-2-one that was used as-is for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07741479B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-2ebc823aa2a444a6b9c4d7143702c9ef |
| Source note | uspto-grants-2010_06 |