HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081712Generated: October 26, 2026
Formaldehyde → 5-[2-(Methylsulfonylamino)ethylthio]3-morpholinomethylimidazo[1,2-a]pyridine
https://huagongshe.com/reaction/1081712
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 5-[2-(Methylsulfonylamino)ethylthio]imidazo[1,2-a]pyridine | HCID 15229363 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-[2-(Methylsulfonylamino)ethylthio]3-morpholinomethylimidazo[1,2-a]pyridine | HCID 23362851 | 71.5% |
Reaction Steps
To a solution of 37% formalin (178 mg, 2.2 mmoles) in acetic acid (2 ml) was added morpholin (192 μl, 2.2 mmoles) under ice-cooling with stirring and the mixture was stirred at room temperature for 30 minutes. 5-[2-(methylsulfonylamino)ethylthio]imidazo[1,2-a]pyridine (543 mg, 2 mmoles) was added to the reaction mixture, followed by stirring at 60° C. for 2 hours. After the solvent was distilled off, the residue was dissolved in chloroform (50 ml) and washed with 1N NaOH (10 ml). Then, the aqueous layer was extracted with chloroform (30 ml×3) and the combined chloroform layer was dried over anhydrous magnesium sulfate, and then the solvent was distilled off. The residue was purified by column chromatography (eluent: ethanol/ethyl acetate=1:10→1:5) to obtain 530 mg of the desired product (71.5%, colorless solid).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05587383 |
|---|
| Source dataset | uspto-grants-1996_12 |
|---|
| ORD ID | ord-e05830de9ec74d43a4d9eff74eb3a55f |
|---|
| Source note | uspto-grants-1996_12 |
|---|