HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 57939120, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | HCID 20826112 | HCID 20826112 | — |
| Product | HCID 57939120 | HCID 57939120 | — |
Reaction Steps
Acryloylchloride (0.27 g, 3.0 mmol) is added dropwise and below 20° C. to a solution of 0.98 g (1.5 mmol) of 2-(2,6-Diethyl-4-hydroxy-2,3,6-trimethyl-piperidin-1-yloxy)-N-{6-[2-(2,6-diethyl-4-hydroxy-2,3,6-trimethyl-piperidin-1-yloxy)-propionylamino]-hexyl}-propionamide (prepared as described in WO 03/004471 A1, example A3) and 0.3 g (3.0 mmol) triethylamine in 30 ml ethyl acetate. The mixture is stirred for 12 h at room temperature, then washed with 3×10 ml water, dried over Na2SO4 and evaporated. Chromatography of the residue over silica gel with hexane-ethyl acetate (3:2) afford 0.33 g of the title compound as a viscous slightly yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07619050B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-09190b6730994f03a68fed0c71b28e73 |
| Source note | uspto-grants-2009_11 |