HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(4-Aminomethyl-phenoxy)-2-methyl-propionic acid ethyl ester → HCID 67072332, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(4-Aminomethyl-phenoxy)-2-methyl-propionic acid ethyl ester | HCID 16109188 | — |
| Reactant | 2-Methyl-6-(4-trifluoromethyl-phenyl)-nicotinic acid | HCID 21935885 | — |
| Reactant | 2-Methyl-6-(4-trifluoromethyl-phenyl)-nicotinic Acid Methyl Ester | HCID 67072269 | — |
| Product | HCID 67072332 | HCID 67072332 | — |
Reaction Steps
In analogy to the procedures described in example 26B] and 26C], 2-(4-aminomethyl-phenoxy)-2-methyl-propionic acid ethyl ester [PCT Int. Appl. (2002), WO 2002/096895A1] was reacted with 2-methyl-6-(4-trifluoromethyl-phenyl)-nicotinic acid (prepared from 2-methyl-6-(4-trifluoromethyl-phenyl)-nicotinic acid methyl ester (example 1L]) in analogy to the procedure described in example 53B]) to give 2-methyl-2-[4-({[2-methyl-6-(4-trifluoromethyl-phenyl)-pyridine-3-carbonyl]-amino}-methyl)-phenoxy]-propionic acid ethyl ester, which was subsequently saponified to yield the title compound as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07115611B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-ba12b96375f54ce3ab6ce2ad237bb79c |
| Source note | uspto-grants-2006_10 |