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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250829Generated: October 26, 2026

Water → 3-(3'-{3-[2-(4-Fluorophenyl)ethyl]-1-methylureido}biphenyl-4-yl)propanoic acid

https://huagongshe.com/reaction/250829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantMeOH tetrahydrofuranHCID 21899815—
ReactantMethyl 3-(3'-{3-[2-(4-fluorophenyl)ethyl]-1-methylureido}biphenyl-4-yl)propanoateHCID 67272001—
SolventAcetic AcidHCID 176—
Product3-(3'-{3-[2-(4-Fluorophenyl)ethyl]-1-methylureido}biphenyl-4-yl)propanoic acidHCID 5808908084%

Reaction Steps

200 mg (5 mmol, 10 eq) of sodium hydroxide are added to a solution of 221 mg (0.51 mmol, 1 eq) of methyl 3-(3′-{3-[2-(4-fluorophenyl)ethyl]-1-methylureido}biphenyl-4-yl)propanoate in 6 ml of an 8/2 tetrahydrofuran/methanol mixture. The reaction mixture is stirred for 3 hours at room temperature. The reaction is stopped by addition of 10 mL of water and 2 mL of acetic acid and then extracted with ethyl acetate. The organic phases are combined and dried over sodium sulfate. The solvents are evaporated off and the residue is then chromatographed on silica gel (70/30 heptane/ethyl acetate). 180 mg of 3-(3′-{3-[2-(4-fluorophenyl)ethyl]-1-methylureido}biphenyl-4-yl)propanoic acid are obtained (m.p.=146° C.). Yield=84%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863332B2
Source datasetuspto-grants-2011_01
ORD IDord-5e7f5f2dce8d49abb997ca636a051763
Source noteuspto-grants-2011_01