HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glycine tert-butyl ester → Tert-butyl 2-(2-cyano-6-(trifluoromethyl)quinolin-4-ylamino)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glycine tert-butyl ester | HCID 151417 | — |
| Reactant | PyBroP | HCID 2733179 | — |
| Reactant | 2-Quinolinecarbonitrile, 4-hydroxy-6-(trifluoromethyl)- | HCID 178510235 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Tert-butyl 2-(2-cyano-6-(trifluoromethyl)quinolin-4-ylamino)acetate | HCID 58562608 | — |
Reaction Steps
To a solution of 4-hydroxy-6-(trifluoromethyl)quinoline-2-carbonitrile (2 g, 8.4 mmol) from example 21, step D, in dry dioxane was added TEA (2.9 mL, 21 mmol) and PyBroP (4.75 g, 10 mmol) and stirred at 50 C for 2 hour. To this solution tert-butyl 2-aminoacetate (1.3 g, 10.1 mmol) was added and stirred at 30° C. for 24 h. The solution was concentrated in vacuo. Water was added to the residue and extracted with EtOAc. The ethyl acetate was removed under vacuum and the residue was purified by flash chromatography (silica gel, 0 to 80% EtOAc in hexane) to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08518969B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-5300833c7104425298df5304595366a2 |
| Source note | uspto-grants-2013_08 |