HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2-(4-aminophenoxy)acetate → HCID 86724356, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2-(4-aminophenoxy)acetate | HCID 412616 | — |
| Reactant | HCID 86724332 | HCID 86724332 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 86724356 | HCID 86724356 | 19.5% |
Reaction Steps
A solution of ethyl 2-(4-aminophenoxy)acetate (0.801 g) and N-(3-((2-chloro-5-fluoropyrimidin-4-yl)amino)phenyl)acrylamide (1.0 g) in 1-butanol (10 mL) was heated to 135° C. for 2 hr. The reaction was monitored on TLC using hexanes:ethyl acetate (3:7) as mobile phase. After completion of the reaction, butanol was removed under reduced pressure and water was added. The mixture was extracted with ethyl acetate and the organic layer was dried over sodium sulfate and solvent was removed under reduced pressure. Crude material was purified by Combiflash chromatography and eluted with 29% ethyl acetate in hexane to give 0.30 g of ethyl 2-(4-((4-((3-acrylamidophenyl)amino)-5-fluoropyrimidin-2-yl)amino)phenoxy)acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09126950B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-5b87422e518f4e30a58232ff3267507f |
| Source note | uspto-grants-2015_09 |