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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709617Generated: October 31, 2026

Water → Ethyl 3-cyclopropyl-3-(6-(((5-(2-fluoro-5-methoxyphenyl)-6-isobutoxypyridin-2-yl)methyl)amino)pyrimidin-4-yl)propanoate

https://huagongshe.com/reaction/709617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(5-(2-Fluoro-5-methoxyphenyl)-6-isobutoxypyridin-2-yl)methanamineHCID 117759972—
ReactantEthyl 3-(6-chloropyrimidin-4-yl)-3-cyclopropylpropanoateHCID 117760030—
SolventAcetonitrileHCID 6342—
ProductEthyl 3-cyclopropyl-3-(6-(((5-(2-fluoro-5-methoxyphenyl)-6-isobutoxypyridin-2-yl)methyl)amino)pyrimidin-4-yl)propanoateHCID 11776016254.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 1-(5-(2-fluoro-5-methoxyphenyl)-6-isobutoxypyridin-2-yl)methanamine (56 mg) and ethyl 3-(6-chloropyrimidin-4-yl)-3-cyclopropylpropanoate (137 mg) in acetonitrile (3.0 mL) was added N,N-diisopropylethylamine (96 μL), and the mixture was stirred at 70° C. for 15 hr. Water 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 purified to by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (52 mg) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181186B2
Source datasetuspto-grants-2015_11
ORD IDord-fc7c359e13924c359ac94fc22f2c3551
Source noteuspto-grants-2015_11