HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 3-oxoheptanoate → 2-[3-({2-[4-Butyl-2-(4-trifluoromethyl-phenyl)-pyrimidin-5-yl]-acetyl}-methyl-amino)-phenoxy]-2-methyl-propionic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 3-oxoheptanoate | HCID 559036 | — |
| Reactant | [4-Butyl-2-(4-trifluoromethyl-phenyl)-pyrimidin-5-yl]-acetic acid | HCID 21935713 | — |
| Reactant | 2-Methyl-2-(3-methylamino-phenoxy)-propionic acid ethyl ester | HCID 67072118 | — |
| Product | 2-[3-({2-[4-Butyl-2-(4-trifluoromethyl-phenyl)-pyrimidin-5-yl]-acetyl}-methyl-amino)-phenoxy]-2-methyl-propionic acid ethyl ester | HCID 67072397 | — |
Reaction Steps
In analogy to the procedures described in example 26B] and 26C], 2-methyl-2-(3-methylamino-phenoxy)-propionic acid ethyl ester (example 26 A]) was reacted with [4-butyl-2-(4-trifluoromethyl-phenyl)-pyrimidin-5-yl]-acetic acid (prepared starting from 3-oxo-heptanoic acid ethyl ester in analogy to the sequences described in examples 27C] to 27F] and examples 26D] and 26E]) to give 2-[3-({2-[4-butyl-2-(4-trifluoromethyl-phenyl)-pyrimidin-5-yl]-acetyl}-methyl-amino)-phenoxy]-2-methyl-propionic acid ethyl ester, which was subsequently saponified to yield the title compound as light yellow amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07115611B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-ee3e5fda1f014b38aa53672edc108e89 |
| Source note | uspto-grants-2006_10 |