HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → Ethyl 2-((2-(tert-butoxycarbonyl(prop-2-ynyl)amino)ethyl)(isopropyl)amino)-2-oxoacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Butanoyl chloride, 2-oxo- | HCID 11007880 | — |
| Reactant | Tert-butyl 2-(isopropylamino)ethyl(prop-2-ynyl)carbamate | HCID 58124856 | — |
| Product | Ethyl 2-((2-(tert-butoxycarbonyl(prop-2-ynyl)amino)ethyl)(isopropyl)amino)-2-oxoacetate | HCID 58124862 | — |
Reaction Steps
To a solution of 900 mg of 10f and 1 ml of triethyl amine in 10 ml of ether was added at 0° C. a solution of 500 μl of ethyloxalyl chloride in 5 ml of ether. The reaction mixture was stirred for ½ h and then quenched by addition of 5% aq. NH4Cl and extracted with ethyl acetate. The organic layers were combined and washed with 1M K2CO3 and water, dried and concentrated, to give 1.03 g of 10g as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08431564B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-afc95efe5f61413591957044f617a8de |
| Source note | uspto-grants-2013_04 |