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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564530Generated: October 29, 2026

Hydrochloric Acid → 3-{[({6-Fluoro-3'-[(4-methyl-1-piperazinyl)methyl]-3-biphenylyl}methyl)(methyl)amino]carbonyl}benzoic Acid

https://huagongshe.com/reaction/564530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantMethyl 3-{[({6-fluoro-3'-[(4-methyl-1-piperazinyl)methyl]-3-biphenylyl}methyl)(methyl)amino]carbonyl}benzoateHCID 57813387—
SolventMethanol--water (1/1)HCID 22242641—
Product3-{[({6-Fluoro-3'-[(4-methyl-1-piperazinyl)methyl]-3-biphenylyl}methyl)(methyl)amino]carbonyl}benzoic AcidHCID 57813343113.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of methyl 3-{[({6-fluoro-3′-[(4-methyl-1-piperazinyl)methyl]-3-biphenylyl}methyl)(methyl)amino]carbonyl}benzoate (0.20 g, 0.409 mmol) in MeOH/H2O (1.2/0.6 mL) was added LiOH.H2O (0.086 g, 2.05 mmol). The mixture was heated in a microwave at 80° C. for 30 min following which it was acidified with HCl, concentrated and the concentrate purified using a Gilson HPLC to afford the title compound 0.221 g (quantitative). LC-MS m/z 476 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067408B2
Source datasetuspto-grants-2011_11
ORD IDord-3cf6cb01a7d046bda305a34ec4ed2e9b
Source noteuspto-grants-2011_11