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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024523Generated: November 1, 2026

Hydrochloric Acid → [(4-(4-Methyl-phenyl)pyridine-2-carbonyl)-amino]-acetic acid

https://huagongshe.com/reaction/1024523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant[(4-(4-Methylphenyl)pyridine-2-carbonyl)amino]-acetic acid methyl esterHCID 24891097—
SolventTetrahydrofuranHCID 8028—
Product[(4-(4-Methyl-phenyl)pyridine-2-carbonyl)-amino]-acetic acidHCID 2489114912%

Reaction Steps

To a solution of [(4-(4-methyl-phenyl)pyridine-2-carbonyl)-amino]-acetic acid methyl ester, 24, (0.092 g, 0.32 mmol) in THF (2 mL) at room temperature is added H2O (1 mL) and LiOH.H2O (0.027 g, 0.64 mmol). The reaction is stirred for 16 hours after which time the solution is acidified using 1M HCl. The solvents are removed under reduced pressure and the solid that remains is suspended in a mixture of THF: MeOH and filtered. The filtrate is concentrated under reduced pressure and the resulting solid is triturated with MeOH and collected by filtration to provide 0.012 g (12% yield) of the desired compound as a colorless solid. 1H NMR (250 MHz, MeOD) δ ppm 8.69 (1H, d, J=4.8 Hz), 8.38 (1H, s), 7.86 (1H, d, J=6.2 Hz), 7.72 (2H, d, J=8.1 Hz), 7.38 (1H, d, J=7.9 Hz), 4.21 (1H, s), 2.44 (2H, s). HPLC-MS: m/z 271 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722895B2
Source datasetuspto-grants-2014_05
ORD IDord-73658e3b69164e94b4c85d0307a55c16
Source noteuspto-grants-2014_05