HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908302Generated: October 28, 2026
Hydrochloric Acid → [(4-(4-Methyl-phenyl)pyridine-2-carbonyl)-amino]-acetic acid
https://huagongshe.com/reaction/1908302
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | [(4-(4-Methylphenyl)pyridine-2-carbonyl)amino]-acetic acid methyl ester | HCID 24891097 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [(4-(4-Methyl-phenyl)pyridine-2-carbonyl)-amino]-acetic acid | HCID 24891149 | 12% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08598210B2 |
|---|
| Source dataset | uspto-grants-2013_12 |
|---|
| ORD ID | ord-faae75825864439eb136a1476e93362a |
|---|
| Source note | uspto-grants-2013_12 |
|---|