HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetaldehyde → 5-(4-Hydroxybutylthio)imidazo[1,2-c]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetaldehyde | HCID 33 | — |
| Reactant | 4-Amino-2-(4-hydroxybutylthio)pyrimidine | HCID 18936811 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-(4-Hydroxybutylthio)imidazo[1,2-c]pyrimidine | HCID 18936882 | — |
Reaction Steps
To a solution of 4.98 g (25 mmol) of 4-amino-2-(4-hydroxybutylthio)pyrimidine in 70 ml of ethanol, 30 ml of a 40% chloroacetaldehyde solution was added, followed by refluxing for 4 hours. After the reaction mixture was cooled, the solvent was distilled off. The residue was dissolved in chloroform, washed with saturated aqueous sodium hydrogen carbonate and dried, after which the solvent was distilled off. The residue was purified by column chromatography (eluent, n-hexane/ethyl acetate=1/1→1/4→ethyl acetate) to yield 3.15 g (56.4%, white crystal) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05840732 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-b32d3089c842437fb6246ce71bf7e620 |
| Source note | uspto-grants-1998_11 |