HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 1-(S)-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethyl amine hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 1-Bromo-2-butanone | HCID 13156 | — |
| Reactant | [2-(4-nitrophenyl)-1-(S)-thiocarbamoylethyl]carbamic acid tert-butyl ester | HCID 57943188 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(S)-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethyl amine hydrobromide | HCID 66694935 | — |
Reaction Steps
A mixture of [2-(4-nitrophenyl)-1-(S)-thiocarbamoylethyl]-carbamic acid tert-butyl ester, 2, (10 g, 30.7 mmol) and 1-bromo-2-butanone (90%, 3.8 mL, 33.8 mmol) in CH3CN (500 mL) is refluxed for 18 hours. The reaction mixture is cooled to room temperature and diethyl ether is added to the solution and the precipitate which forms is removed by filtration to afford 7.47 g of the desired product. ESI+ MS 278 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08106078B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-91abbc189ed14c3c82288f4f8278b205 |
| Source note | uspto-grants-2012_01 |