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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709618Generated: October 31, 2026

Hydrochloric Acid → 3-Cyclopropyl-3-(6-(((5-(2-fluoro-5-methoxyphenyl)-6-isobutoxypyridin-2-yl)methyl)amino)pyrimidin-4-yl)propanoic acid

https://huagongshe.com/reaction/709618

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 3-cyclopropyl-3-(6-(((5-(2-fluoro-5-methoxyphenyl)-6-isobutoxypyridin-2-yl)methyl)amino)pyrimidin-4-yl)propanoateHCID 117760162—
SolventMethanolHCID 887—
Product3-Cyclopropyl-3-(6-(((5-(2-fluoro-5-methoxyphenyl)-6-isobutoxypyridin-2-yl)methyl)amino)pyrimidin-4-yl)propanoic acidHCID 11776023882.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of ethyl 3-cyclopropyl-3-(6-(((5-(2-fluoro-5-methoxyphenyl)-6-isobutoxypyridin-2-yl)methyl)amino)pyrimidin-4-yl)propanoate (65 mg) in methanol (5.0 mL) was added 1N aqueous sodium hydroxide solution (0.37 mL), and the mixture was stirred at 50° C. for 15 hr. 1N Hydrochloric acid was added, and the reaction mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was recrystallized from hexane/diethyl ether to give the title compound (51 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181186B2
Source datasetuspto-grants-2015_11
ORD IDord-aa1497b573704fffaaf5af16e8b9a3ea
Source noteuspto-grants-2015_11