Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661490Generated: October 30, 2026

Glycine methyl ester hydrochloride → HCID 54749369, compound

https://huagongshe.com/reaction/1661490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycine methyl ester hydrochlorideHCID 122755—
Reactant83179-00-4HCID 57744891—
ReactantHCID 67429156HCID 67429156—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 54749369HCID 54749369—

Reaction Conditions

Temperature100 °C

Reaction Steps

Methyl 2-(7-hydroxy-4-methyl-5-oxo-4,5-dihydrothieno[3,2-b]pyridine-6-carboxamido)acetate. A mixture of methyl 2-aminoacetate hydrochloride (291 mg, 2317 μmol) and ethyl 7-hydroxy-4-methyl-5-oxo-4,5-dihydrothieno[3,2-b]pyridine-6-carboxylate (489 mg, 1931 μmol) in 15 mL dioxane was heated to 100° C. in a sealed tube and stirred for 15 hours. The mixture was cooled to room temperature, and the resulting suspension was added dropwise to 100 mL ice-water. The precipitate was collected by filtration, washed with H2O, and dried in vacuo. The solids were triturated with Et2O, collected by filtration, and dried to give a beige solid. Purification of the crude product by flash chromatography (Gradient from hexanes to hexanes/EtOAc=1:1) gave the title compound as a white solid (301 mg). MS (ESI) m/z: Calculated; 296.3: Observed; 297.1. 1H NMR (300 MHz, CDCl3) δ ppm 10.73 (1H, br. s), 7.78 (1H, d, J=5.3 Hz), 7.08 (1H, d, J=5.3 Hz), 4.24 (2H, br. s), 3.79 (3H, s), 3.69 (3H, s)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030346B2
Source datasetuspto-grants-2011_10
ORD IDord-9563c980e84b4592b9414341124ddac5
Source noteuspto-grants-2011_10