HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 86731332, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Ethylhexyl 3-mercaptopropionate | HCID 92640 | — |
| Reactant | tert-Butyl {(2S)-1-[(4-chloro-5-nitropyridin-2-yl)oxy]propan-2-yl}carbamate | HCID 86731217 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86731332 | HCID 86731332 | 96.9% |
Reaction Steps
A mixture of 2-ethylhexyl 3-sulfanylpropanoate (2.17 g), tert-butyl ((2S)-1-((4-chloro-5-nitropyridin-2-yl)oxy)propan-2-yl)carbamate (3.00 g), triethylamine (1.39 mL) and DMF (30 mL) was stirred at room temperature overnight. To the reaction mixture was added water, and the mixture was extracted with ethyl acetate. The combined organic layer were washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (4.50 g). MS (ESI+): [M+H]+ 514.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09133129B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-c2f5917df6ca414e8c0e653287f8154b |
| Source note | uspto-grants-2015_09 |