US2016075636A1PendingUtilityA1
Process for the Preparation of (-)-(4-Chloro-Phenyl)-(3-Trifluoromethyl-Phenoxy)-Acetic Acid 2-Acetylamino-Ethyl Ester
Est. expiryApr 3, 2028(~1.7 yrs left)· nominal 20-yr term from priority
A61P 3/10A61P 3/00C07C 231/12C07B 2200/07C07C 231/24C07B 2200/13C07C 233/51C07C 51/09
45
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Claims
Abstract
The present invention is directed to a novel process for the preparation of (4-chloro-phenyl)-(3-trifluoromethyl-phenoxy)-acetic acid 2-acetylamino-ethyl ester, useful in the treatment of metabolic disorders and further to a process for the preparation of (4-chloro-phenyl)-(3-trifluoromethyl-phenoxy)-acetic acid, a synthesis intermediate.
Claims
exact text as granted — not AI-modified1 .- 57 . (canceled)
58 . A compound that is (−)-4-chlorophenyl-(3-trifluoromethyl-phenoxy)acetic acid 2-acetylamino-ethyl ester in crystalline solid form having an enantiomeric excess of 99.7% to 99.9% and a chemical purity of 99.1% to 99.6%.
59 . The compound of claim 58 having an enantiomeric excess of greater than 99.9% and a chemical purity of 99.9%.
60 . The compound of claim 59 , where the compound has been recrystallized.
61 . The compound of claim 60 , where the compound has been recrystallized from a single solvent.
62 . The compound of claim 61 , where the single solvent is diisopropyl ether.
63 . A compound that is (−)-(4-chlorophenyl)-(3-trifluoromethyl-phenoxy)acetic acid in crystalline solid form having an enantiomeric excess of 97.5% to 99.5% and a chemical purity of 97.5% to 99.5%.Cited by (0)
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